MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss-Reference-Cited by-同舟云学术

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Published:2001-09 Issue:3 Volume:69 Page:635-640
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Melchionda Salvatore,Ahituv Nadav,Bisceglia Luigi,Sobe Tama,Glaser Fabian,Rabionet Raquel,Arbones Maria Lourdes,Notarangelo Angelo,Di Iorio Enzo,Carella Massimo,Zelante Leopoldo,Estivill Xavier,Avraham Karen B.,Gasparini Paolo

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. Genomic structure of the human unconventional myosin VI gene;Ahituv;Gene,2000

2. ConSurf: an algorithmic tool for the identification of functional regions in proteins by surface mapping of phylogenetic information;Armon;J Mol Biol,2001

3. The mouse Snell’s waltzer deafness gene encodes an unconventional myosin required for the structural integrity of inner ear hair cells;Avraham;Nat Genet,1995

4. Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice;Avraham;Hum Mol Genet,1997

5. Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families;Coucke;Hum Mol Genet,1999

Cited by 196 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in MYO6 Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss;Genetic Testing and Molecular Biomarkers;2024-08-01

2. Live-cell single-molecule fluorescence microscopy for protruding organelles reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of inner ear hair cells;2024-05-07

3. The two C. elegans class VI myosins, SPE-15/HUM-3 and HUM-8, share similar motor properties, but have distinct developmental and tissue expression patterns;Frontiers in Physiology;2024-04-10

4. Pathophysiology of human hearing loss associated with variants in myosins;Frontiers in Physiology;2024-03-18

5. Breaking genetic shackles: The advance of base editing in genetic disorder treatment;Frontiers in Pharmacology;2024-03-06