These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
125 related articles for article (PubMed ID: 39016090)
1. A case study of Duchenne muscular dystrophy caused by Alu element insertion in Li H; Zhang RY; Li CY; Zhang XL; Zheng QY; Liu XZ Yi Chuan; 2024 Jul; 46(7):570-580. PubMed ID: 39016090 [TBL] [Abstract][Full Text] [Related]
2. Novel Mutation of the Dystrophin Gene in a Child with Duchenne Muscular Dystrophy. Jiang J; Jiang T; Xu J; Shen J; Gao F Fetal Pediatr Pathol; 2018 Feb; 37(1):1-6. PubMed ID: 29336709 [TBL] [Abstract][Full Text] [Related]
3. Novel mutation in exon 56 of the dystrophin gene in a child with Duchenne muscular dystrophy. Zhu JF; Liu HH; Zhou T; Tian L Int J Mol Med; 2013 Nov; 32(5):1166-70. PubMed ID: 24065205 [TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center. Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011 [TBL] [Abstract][Full Text] [Related]
5. Genetic analysis of dystrophin gene for affected male and female carriers with Duchenne/Becker muscular dystrophy in Korea. Lee BL; Nam SH; Lee JH; Ki CS; Lee M; Lee J J Korean Med Sci; 2012 Mar; 27(3):274-80. PubMed ID: 22379338 [TBL] [Abstract][Full Text] [Related]
6. Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community. Elhawary NA; Jiffri EH; Jambi S; Mufti AH; Dannoun A; Kordi H; Khogeer A; Jiffri OH; Elhawary AN; Tayeb MT Hum Genomics; 2018 Apr; 12(1):18. PubMed ID: 29631625 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report. Wang Y; Chen Y; Wang SM; Liu X; Gu YN; Feng Z BMC Med Genet; 2020 Nov; 21(1):222. PubMed ID: 33176713 [TBL] [Abstract][Full Text] [Related]
8. Identification of two novel insertion abnormal transcripts in two Chinese families affected with Dystrophinopathy. Xu Y; Song T; Li Y; Guo F; Jin X; Cheng L; Zheng J; Li C; Zhang Y; Chen B; Zhang J J Clin Lab Anal; 2020 Apr; 34(4):e23142. PubMed ID: 31793735 [TBL] [Abstract][Full Text] [Related]
9. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy]. Bai Y; Li S; Zong YN; Li XL; Zhao ZH; Kong XD Zhonghua Yi Xue Za Zhi; 2016 Apr; 96(16):1261-9. PubMed ID: 27122458 [TBL] [Abstract][Full Text] [Related]
10. Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4. Baskin B; Gibson WT; Ray PN Neuromuscul Disord; 2011 Mar; 21(3):178-82. PubMed ID: 21134752 [TBL] [Abstract][Full Text] [Related]
11. When a mid-intronic variation of DMD gene creates an ESE site. Trabelsi M; Beugnet C; Deburgrave N; Commere V; Orhant L; Leturcq F; Chelly J Neuromuscul Disord; 2014 Dec; 24(12):1111-7. PubMed ID: 25193336 [TBL] [Abstract][Full Text] [Related]
12. Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy. Kapoor S; Bindu PS; Taly AB; Sinha S; Gayathri N; Rani SV; Chandak GR; Kumar A Mol Vis; 2012; 18():2022-32. PubMed ID: 22876130 [TBL] [Abstract][Full Text] [Related]
13. A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping. Walmsley GL; Arechavala-Gomeza V; Fernandez-Fuente M; Burke MM; Nagel N; Holder A; Stanley R; Chandler K; Marks SL; Muntoni F; Shelton GD; Piercy RJ PLoS One; 2010 Jan; 5(1):e8647. PubMed ID: 20072625 [TBL] [Abstract][Full Text] [Related]
14. Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing. Magri F; Del Bo R; D'Angelo MG; Govoni A; Ghezzi S; Gandossini S; Sciacco M; Ciscato P; Bordoni A; Tedeschi S; Fortunato F; Lucchini V; Cereda M; Corti S; Moggio M; Bresolin N; Comi GP BMC Med Genet; 2011 Mar; 12():37. PubMed ID: 21396098 [TBL] [Abstract][Full Text] [Related]
15. Hybrid minigene splicing assay verified the pathogenicity of a novel splice site variant in the dystrophin gene of a Chinese patient with typical Duchenne muscular dystrophy phenotype. Wang Z; Lin Y; Qiu L; Zheng D; Yan A; Zeng J; Lan F Clin Chem Lab Med; 2016 Sep; 54(9):1435-40. PubMed ID: 26985686 [TBL] [Abstract][Full Text] [Related]
16. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials. Anthony K; Cirak S; Torelli S; Tasca G; Feng L; Arechavala-Gomeza V; Armaroli A; Guglieri M; Straathof CS; Verschuuren JJ; Aartsma-Rus A; Helderman-van den Enden P; Bushby K; Straub V; Sewry C; Ferlini A; Ricci E; Morgan JE; Muntoni F Brain; 2011 Dec; 134(Pt 12):3547-59. PubMed ID: 22102647 [TBL] [Abstract][Full Text] [Related]
17. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach. Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831 [TBL] [Abstract][Full Text] [Related]
18. A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathy. Dwianingsih EK; Malueka RG; Nishida A; Itoh K; Lee T; Yagi M; Iijima K; Takeshima Y; Matsuo M J Hum Genet; 2014 Aug; 59(8):423-9. PubMed ID: 24871807 [TBL] [Abstract][Full Text] [Related]
19. A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy. Lo IF; Lai KK; Tong TM; Lam ST Chin Med J (Engl); 2006 Jul; 119(13):1079-87. PubMed ID: 16834926 [TBL] [Abstract][Full Text] [Related]
20. Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping. Anthony K; Arechavala-Gomeza V; Ricotti V; Torelli S; Feng L; Janghra N; Tasca G; Guglieri M; Barresi R; Armaroli A; Ferlini A; Bushby K; Straub V; Ricci E; Sewry C; Morgan J; Muntoni F JAMA Neurol; 2014 Jan; 71(1):32-40. PubMed ID: 24217213 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]