95 related articles for article (PubMed ID: 10596456)
1. Linkage disequilibrium between IDUA kpnI-VNTR haplotype in Mexican patients with MPS-I.
Gallegos-Arreola M; Rivas-Solis F; Flores-Martínez S; Zúñiga-González G; Sandoval-Ramírez L; Cantú-Garza JM; Ranaji C; Figuera L; Morán-Moguel MC; Sánchez Corona J
Arch Med Res; 1999; 30(5):375-9. PubMed ID: 10596456
[TBL] [Abstract][Full Text] [Related]
2. Mucopolysaccharidosis I: a comparative study of haplotypes Eco47III-NspI sites frequencies in patients and healthy subjects of Mexican population.
Gallegos-Arreola MP; Arnaud-López L; Figuera LE; Beltrán Jaramillo TS; Rangel-Villalobos H; Thomatsu S; Zúñiga-González GM
Ann Genet; 2003; 46(1):7-10. PubMed ID: 12818523
[TBL] [Abstract][Full Text] [Related]
3. Haplotypes Eco47 III-Nsp I sites frequencies on the IDUA gene in Mexican native population.
Gallegos-Arreola MP; Sandoval-Ramírez L; Figuera LE; Arnaud-López L; Rivas F; Mariaud-Schmidt RP; Zúñiga-González GM
Eur J Med Genet; 2005; 48(1):29-32. PubMed ID: 15953403
[TBL] [Abstract][Full Text] [Related]
4. Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele.
Scott HS; Nelson PV; Cooper A; Wraith JE; Hopwood JJ; Morris CP
Hum Genet; 1992 Mar; 88(6):701-2. PubMed ID: 1551679
[TBL] [Abstract][Full Text] [Related]
5. alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype.
Scott HS; Litjens T; Nelson PV; Brooks DA; Hopwood JJ; Morris CP
Hum Mutat; 1992; 1(4):333-9. PubMed ID: 1301941
[TBL] [Abstract][Full Text] [Related]
6. Identification and molecular characterization of alpha-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy.
Yogalingam G; Guo XH; Muller VJ; Brooks DA; Clements PR; Kakkis ED; Hopwood JJ
Hum Mutat; 2004 Sep; 24(3):199-207. PubMed ID: 15300847
[TBL] [Abstract][Full Text] [Related]
7. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.
Scott HS; Bunge S; Gal A; Clarke LA; Morris CP; Hopwood JJ
Hum Mutat; 1995; 6(4):288-302. PubMed ID: 8680403
[TBL] [Abstract][Full Text] [Related]
8. Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations.
Yamagishi A; Tomatsu S; Fukuda S; Uchiyama A; Shimozawa N; Suzuki Y; Kondo N; Sukegawa K; Orii T
Hum Mutat; 1996; 7(1):23-9. PubMed ID: 8664897
[TBL] [Abstract][Full Text] [Related]
9. Diversity of mutations and distribution of single nucleotide polymorphic alleles in the human alpha-L-iduronidase (IDUA) gene.
Li P; Wood T; Thompson JN
Genet Med; 2002; 4(6):420-6. PubMed ID: 12509712
[TBL] [Abstract][Full Text] [Related]
10. Human alpha-L-iduronidase (IDUA) gene: apparent recombination in intron 2 by haplotype analysis in a Taiwanese population.
Lee-Chen GJ; Wang TR; Hwu WL; Day KR; Wang CK
J Formos Med Assoc; 1998 Jul; 97(7):465-70. PubMed ID: 9700243
[TBL] [Abstract][Full Text] [Related]
11. A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotype.
Scott HS; Litjens T; Hopwood JJ; Morris CP
Hum Mutat; 1992; 1(2):103-8. PubMed ID: 1301196
[TBL] [Abstract][Full Text] [Related]
12. p.X654R IDUA variant among Thai individuals with intermediate mucopolysaccharidosis type I and its residual activity as demonstrated in COS-7 cells.
Ngiwsara L; Ketudat-Cairns JR; Sawangareetrakul P; Charoenwattanasatien R; Champattanachai V; Kuptanon C; Pangkanon S; Tim-Aroon T; Wattanasirichaigoon D; Svasti J
Ann Hum Genet; 2018 May; 82(3):150-157. PubMed ID: 29282708
[TBL] [Abstract][Full Text] [Related]
13. Human alpha-L-iduronidase (IDUA) gene: correlation of polymorphic DNA haplotype and IDUA activity in Chinese population.
Lee-Chen GJ; Wang CK; Huang SF; Day KR
Proc Natl Sci Counc Repub China B; 1998 Jan; 22(1):31-8. PubMed ID: 9536518
[TBL] [Abstract][Full Text] [Related]
14. Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRs.
Rangel-Villalobos H; Rivas F; Sandoval L; Ibarra B; Garcìa-Carvajal ZY; Cantú JM; Figuera LE
Hum Biol; 2000 Dec; 72(6):983-95. PubMed ID: 11236868
[TBL] [Abstract][Full Text] [Related]
15. Clinical and Molecular Characterization of Patients with Mucopolysaccharidosis Type I in an Algerian Series.
Tebani A; Zanoutene-Cheriet L; Adjtoutah Z; Abily-Donval L; Brasse-Lagnel C; Laquerrière A; Marret S; Chalabi Benabdellah A; Bekri S
Int J Mol Sci; 2016 May; 17(5):. PubMed ID: 27196898
[TBL] [Abstract][Full Text] [Related]
16. Renin gene haplotype diversity and linkage disequilibrium in two Mexican and one German population samples.
Valdez-Velazquez LL; Mendoza-Carrera F; Perez-Parra SA; Rodarte-Hurtado K; Sandoval-Ramirez L; Montoya-Fuentes H; Quintero-Ramos A; Delgado-Enciso I; Montes-Galindo DA; Gomez-Sandoval Z; Olivares N; Rivas F
J Renin Angiotensin Aldosterone Syst; 2011 Sep; 12(3):231-7. PubMed ID: 21163863
[TBL] [Abstract][Full Text] [Related]
17. Mutational Analysis of the alpha-L-iduronidase gene in three Egyptian families: identification of three novel mutations and five novel polymorphisms.
Amr K; Katoury A; Abdel-Hamid M; Bassiouni R; Ibrahim M; Fateen E
Genet Test Mol Biomarkers; 2009 Dec; 13(6):761-4. PubMed ID: 19839758
[TBL] [Abstract][Full Text] [Related]
18. Linkage disequilibrium between four MTTP gene polymorphisms in a Mexican population.
Luévano KE; González JR; Perea FJ; Magaña MT
Ann Hum Biol; 2009; 36(2):211-9. PubMed ID: 19255880
[TBL] [Abstract][Full Text] [Related]
19. Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome.
Chkioua L; Boudabous H; Jaballi I; Grissa O; Turkia HB; Tebib N; Laradi S
Diagn Pathol; 2018 May; 13(1):35. PubMed ID: 29843745
[TBL] [Abstract][Full Text] [Related]
20. [Mutation analysis and prenatal diagnosis of 2 cases with mucopolysaccharidosis type I].
Wang XN; Wei M; Shi HP; Qiu ZQ; Yao FX; Meng Y; Zhang WM
Zhonghua Er Ke Za Zhi; 2011 Apr; 49(4):306-10. PubMed ID: 21624210
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]