- Title
- Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
- Creators
- Oscar Diaz-HortaDuygu DumanJoseph FosterAslı SırmacıMichael GonzalezNejat MahdiehNikou FotouhiMortaza BonyadiFiliz Başak CengizIbis MenendezRick H UlloaYvonne J. K EdwardsStephan ZüchnerSusan BlantonMustafa Tekin
- Contributors
- Andreas R Janecke (Editor)
- Publication Details
- PloS one, Vol.8(5)
- Academic Unit
- Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics - Clinical and Translational Genetics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Language
- English
- Resource Type
- Journal article
- PMCID
- PMC3660617
- Record Identifier
- 991031599523102976
Journal article
Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
PloS one, Vol.8(5)
2013-05-17
PMCID: PMC3660617
Appears in UM Open Access Research Published in PloS
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