Open AccessCorrection: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
Author(s) -
Oscar DiazHorta,
Duygu Duman,
Joseph Foster,
Aslı Sırmacı,
Michael Gonzalez,
Nejat Mahdieh,
Nikou Fotouhi,
Mortaza Bonyadi,
Filiz Başak Cengiz,
Ibis Menéndez,
Rick H. Ulloa,
Yvonne J. K. Edwards,
Stephan Züchner,
Susan H. Blanton,
Mustafa Tekin
Publication year - 2013
Publication title -
plos one
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd
Subject(s) - exome sequencing , genetics , exome , hearing loss , biology , computational biology , mutation , medicine , gene , audiology