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.
47. A novel homozygous MYO7A mutation involved in a Venezuelan population with high frequency of USHER1B. Guzmán HO; Palacios AM; De Almada MI; Utrera RA Ophthalmic Genet; 2016 Sep; 37(3):328-30. PubMed ID: 26864046 [TBL] [Abstract][Full Text] [Related]
48. Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I. Zhou Q; Lenger C; Smith R; Kimberling WJ; Ye M; Lehmann O; MacDonald I Mol Vis; 2012; 18():1379-83. PubMed ID: 22690115 [TBL] [Abstract][Full Text] [Related]
49. Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity. Janecke AR; Meins M; Sadeghi M; Grundmann K; Apfelstedt-Sylla E; Zrenner E; Rosenberg T; Gal A Hum Mutat; 1999; 13(2):133-40. PubMed ID: 10094549 [TBL] [Abstract][Full Text] [Related]
50. Identification of three novel mutations in the MYO7A gene. Cuevas JM; Espinós C; Millán JM; Sánchez F; Trujillo MJ; Ayuso C; Beneyto M; Nájera C Hum Mutat; 1999 Aug; 14(2):181. PubMed ID: 10447383 [TBL] [Abstract][Full Text] [Related]
51. Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. Weston MD; Kelley PM; Overbeck LD; Wagenaar M; Orten DJ; Hasson T; Chen ZY; Corey D; Mooseker M; Sumegi J; Cremers C; Moller C; Jacobson SG; Gorin MB; Kimberling WJ Am J Hum Genet; 1996 Nov; 59(5):1074-83. PubMed ID: 8900236 [TBL] [Abstract][Full Text] [Related]
52. Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I. Jaijo T; Aller E; Oltra S; Beneyto M; Nájera C; Ayuso C; Baiget M; Carballo M; Antiñolo G; Valverde D; Moreno F; Vilela C; Perez-Garrigues H; Navea A; Millán JM Hum Mutat; 2006 Mar; 27(3):290-1. PubMed ID: 16470552 [TBL] [Abstract][Full Text] [Related]
53. Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells. Tang ZH; Chen JR; Zheng J; Shi HS; Ding J; Qian XD; Zhang C; Chen JL; Wang CC; Li L; Chen JZ; Yin SK; Huang TS; Chen P; Guan MX; Wang JF Stem Cells Transl Med; 2016 May; 5(5):561-71. PubMed ID: 27013738 [TBL] [Abstract][Full Text] [Related]
54. Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11). Bolz H; Bolz SS; Schade G; Kothe C; Mohrmann G; Hess M; Gal A Hum Mutat; 2004 Sep; 24(3):274-5. PubMed ID: 15300860 [TBL] [Abstract][Full Text] [Related]
55. Inner ear morphology is perturbed in two novel mouse models of recessive deafness. Miller KA; Williams LH; Rose E; Kuiper M; Dahl HH; Manji SS PLoS One; 2012; 7(12):e51284. PubMed ID: 23251483 [TBL] [Abstract][Full Text] [Related]
56. The genetic dissection of Lu Y; Zhou D; King R; Zhu S; Simpson CL; Jones BC; Zhang W; Geisert EE; Lu L Mol Vis; 2018; 24():115-126. PubMed ID: 29430167 [TBL] [Abstract][Full Text] [Related]
57. [Research progress of mutational spectrum and pathophysiology of WFS1 gene in Wolfram syndrome and nonsyndromic low frequency sensorineural hearing loss]. Shi SM; Han YH; Wang HB Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Sep; 51(9):712-715. PubMed ID: 27666717 [TBL] [Abstract][Full Text] [Related]
58. [Analysis of MYO7A gene mutation in a family with non-syndromic autosomal recessive deafness]. Wang S; Qin L; Ding K; Hao B; Bian S; Wang Z; Wang Q; Wang X; Zhang W; Liao S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):965-969. PubMed ID: 31598937 [TBL] [Abstract][Full Text] [Related]
59. Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome. Espinós C; Millán JM; Sánchez F; Beneyto M; Nájera C Hum Genet; 1998 Jun; 102(6):691-4. PubMed ID: 9703432 [TBL] [Abstract][Full Text] [Related]
60. Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree. Kooshavar D; Razipour M; Movasat M; Keramatipour M Int J Pediatr Otorhinolaryngol; 2018 Jan; 104():10-13. PubMed ID: 29287847 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]