Elie El‐Zir

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 · 635 citations · Full text

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon et al. · Nature Genetics · 1999 · 575 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23

H. Chaib, Christophe Place, Nabiha Salem et al. · Human Molecular Genetics · 1996 · 83 citations

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36

Mirna Mustapha, Sébastien Chardenoux, Alexandre Nieder et al. · European Journal of Human Genetics · 1998 · 43 citations · Full text

Developmental Anomaly, Isolated Deafness, Developmental Biology +10

Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness

Mirna Mustapha, Nabiha Salem, Dominique Weil et al. · European Journal of Human Genetics · 1998 · 26 citations · Full text

Auditory Processing, Mendelian Disorder, Genetic Disorder +8