Concepedia

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

Sébastien Albert, Hélène Blons, Laurence Jonard, Delphine Feldmann, Pierre Chauvin, N. Loundon, Annie Sergent-Allaoui, Muriel Houang, Alain Joannard, S. Schmerber,

European Journal of Human Genetics · 2006 · 243 citations · 19 references

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19

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Lorraine A. Everett, Benjamin Gläser, John C. Beck et al. · Nature Genetics · 1997 · 1.1K citations

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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 636 citations · Full text

, , +11

The Pendred syndrome gene encodes a chloride-iodide transport protein

Daryl A. Scott, Rong Wang, Trisha Kreman et al. · Nature Genetics · 1999 · 567 citations

, , +10

Origins and frequencies of <i>SLC26A4</i> (<i>PDS</i>) mutations in east and south Asians: global implications for the epidemiology of deafness

Journal of Medical Genetics · 2003 · 322 citations · Full text

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Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

Shin‐ichi Usami, Satoko Abe, Mike D. Weston et al. · Human Genetics · 1999 · 316 citations

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