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.
82 related articles for article (PubMed ID: 22911656)
1. A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect. Abdelfatah N; Merner N; Houston J; Benteau T; Griffin A; Doucette L; Stockley T; Lauzon JL; Young TL Hum Mutat; 2013 Jan; 34(1):66-9. PubMed ID: 22911656 [TBL] [Abstract][Full Text] [Related]
2. A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss. Niu Z; Yan D; Bressler S; Mei L; Feng Y; Liu X Int J Pediatr Otorhinolaryngol; 2018 Jan; 104():47-50. PubMed ID: 29287879 [TBL] [Abstract][Full Text] [Related]
3. A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. Niu Z; Feng Y; Mei L; Sun J; Wang X; Wang J; Hu Z; Dong Y; Chen H; He C; Liu Y; Cai X; Liu X; Jiang L PLoS One; 2017; 12(5):e0178384. PubMed ID: 28542515 [TBL] [Abstract][Full Text] [Related]
4. Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. Schraders M; Haas SA; Weegerink NJ; Oostrik J; Hu H; Hoefsloot LH; Kannan S; Huygen PL; Pennings RJ; Admiraal RJ; Kalscheuer VM; Kunst HP; Kremer H Am J Hum Genet; 2011 May; 88(5):628-34. PubMed ID: 21549342 [TBL] [Abstract][Full Text] [Related]
5. Alport syndrome. Molecular genetic aspects. Hertz JM Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970 [TBL] [Abstract][Full Text] [Related]
6. X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care. Stanton SG; Griffin A; Stockley TL; Brown C; Young TL; Benteau T; Abdelfatah N Am J Audiol; 2014 Jun; 23(2):190-200. PubMed ID: 24687041 [TBL] [Abstract][Full Text] [Related]
7. Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Huebner AK; Gandia M; Frommolt P; Maak A; Wicklein EM; Thiele H; Altmüller J; Wagner F; Viñuela A; Aguirre LA; Moreno F; Maier H; Rau I; Giesselmann S; Nürnberg G; Gal A; Nürnberg P; Hübner CA; del Castillo I; Kurth I Am J Hum Genet; 2011 May; 88(5):621-7. PubMed ID: 21549336 [TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing identifies a donor splice-site variant in SMPX that causes rare X-linked congenital deafness. Lv Y; Gu J; Qiu H; Li H; Zhang Z; Yin S; Mao Y; Kong L; Liang B; Jiang H; Liu C Mol Genet Genomic Med; 2019 Nov; 7(11):e967. PubMed ID: 31478598 [TBL] [Abstract][Full Text] [Related]
9. A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss. Hilgert N; Topsakal V; van Dinther J; Offeciers E; Van de Heyning P; Van Camp G Eur J Hum Genet; 2008 May; 16(5):593-602. PubMed ID: 18212818 [TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family. Deng Y; Niu Z; Fan L; Ling J; Chen H; Cai X; Mei L; He C; Zhang X; Wen J; Li M; Li W; Li T; Sang S; Liu Y; Feng Y J Hum Genet; 2018 Jun; 63(6):723-730. PubMed ID: 29559740 [TBL] [Abstract][Full Text] [Related]
11. Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene. Dykxhoorn DM; Tong X; Gosstola NC; Liu XZ Stem Cell Res; 2021 Jul; 54():102405. PubMed ID: 34052664 [TBL] [Abstract][Full Text] [Related]
12. [Analysis of SEDL gene mutation in a Chinese pedigree with X-linked spondyloepiphyseal dysplasia tarda]. Li J; Chai X; Lu L; Zhu J; Du X; Zhao L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):604-7. PubMed ID: 25297591 [TBL] [Abstract][Full Text] [Related]
13. Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmus. Fingert JH; Roos B; Eyestone ME; Pham JD; Mellot ML; Stone E Ophthalmic Genet; 2010 Jun; 31(2):77-80. PubMed ID: 20450309 [TBL] [Abstract][Full Text] [Related]
14. Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer. Collin RW; de Heer AM; Oostrik J; Pauw RJ; Plantinga RF; Huygen PL; Admiraal R; de Brouwer AP; Strom TM; Cremers CW; Kremer H Eur J Hum Genet; 2008 Dec; 16(12):1430-6. PubMed ID: 18575463 [TBL] [Abstract][Full Text] [Related]
15. A common NYX mutation in Flemish patients with X linked CSNB. Leroy BP; Budde BS; Wittmer M; De Baere E; Berger W; Zeitz C Br J Ophthalmol; 2009 May; 93(5):692-6. PubMed ID: 18617546 [TBL] [Abstract][Full Text] [Related]
16. Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA. Song MH; Lee HK; Choi JY; Kim S; Bok J; Kim UK Clin Genet; 2010 Dec; 78(6):524-32. PubMed ID: 20412083 [TBL] [Abstract][Full Text] [Related]
17. Two mutations in exon XII of the protein S alpha gene in four thrombophilic families resulting in premature stop codons and depressed levels of mutated mRNA. Andersen BD; Lind B; Philips M; Hansen AB; Ingerslev J; Thorsen S Thromb Haemost; 1996 Aug; 76(2):143-50. PubMed ID: 8865520 [TBL] [Abstract][Full Text] [Related]
18. A novel CACNA1F gene mutation causes Aland Island eye disease. Jalkanen R; Bech-Hansen NT; Tobias R; Sankila EM; Mäntyjärvi M; Forsius H; de la Chapelle A; Alitalo T Invest Ophthalmol Vis Sci; 2007 Jun; 48(6):2498-502. PubMed ID: 17525176 [TBL] [Abstract][Full Text] [Related]
19. X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7. Shiels A; Bennett TM; Prince JB; Tychsen L Mol Vis; 2007 Nov; 13():2233-41. PubMed ID: 18087240 [TBL] [Abstract][Full Text] [Related]
20. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families. Brownstein Z; Friedman LM; Shahin H; Oron-Karni V; Kol N; Abu Rayyan A; Parzefall T; Lev D; Shalev S; Frydman M; Davidov B; Shohat M; Rahile M; Lieberman S; Levy-Lahad E; Lee MK; Shomron N; King MC; Walsh T; Kanaan M; Avraham KB Genome Biol; 2011 Sep; 12(9):R89. PubMed ID: 21917145 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]