Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Growth and Development Research Center, Tehran University of Medical Sciences, Tehran and Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran Citation: Diaz-Horta O, Duman D, Foster J II, Sırmacı A, Gonzalez M, Mahdieh N, et al. (2013) Correction: Whole-Exome Sequencing Efficiently...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2013-05, Vol.8 (5)
Hauptverfasser: Diaz-Horta, Oscar, Duman, Duygu, Foster, Joseph, Sırmacı, Aslı, Gonzalez, Michael, Mahdieh, Nejat, Fotouhi, Nikou, Bonyadi, Mortaza, Cengiz, Filiz Başak, Menendez, Ibis, Ulloa, Rick H., Edwards, Yvonne J. K., Züchner, Stephan, Blanton, Susan, Tekin, Mustafa
Format: Artikel
Sprache:eng
Schlagworte:
Auditory defects
Hearing loss
Mutation
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Growth and Development Research Center, Tehran University of Medical Sciences, Tehran and Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran Citation: Diaz-Horta O, Duman D, Foster J II, Sırmacı A, Gonzalez M, Mahdieh N, et al. (2013) Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss.
ISSN:1932-6203
1932-6203
DOI:10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd