Repository of Research and Investigative Information

Repository of Research and Investigative Information

Ilam University of Medical Sciences

Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE)

Sun Aug 14 02:04:00 2022

(2013) Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE). Plos One. ISSN 19326203 (ISSN)

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Official URL: https://www.scopus.com/inward/record.uri?eid=2-s2....
Item Type: Article
Creators:
CreatorsEmail
Diaz-Horta, O.UNSPECIFIED
Duman, D.UNSPECIFIED
Foster Ii, J.UNSPECIFIED
Sirmaci, A.UNSPECIFIED
Gonzalez, M.UNSPECIFIED
Mahdieh, N.UNSPECIFIED
Fotouhi, N.UNSPECIFIED
Bonyadi, M.UNSPECIFIED
Cengiz, F. B.UNSPECIFIED
Menendez, I.UNSPECIFIED
Ulloa, R. H.UNSPECIFIED
Edwards, Y. J. K.UNSPECIFIED
Zuc̈hner, S.UNSPECIFIED
Blanton, S.UNSPECIFIED
Tekin, M.UNSPECIFIED
Keywords: erratum error
Divisions:
Journal or Publication Title: Plos One
Journal Index: Scopus
Volume: 8
Number: 5
Identification Number: https://doi.org/10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd
ISSN: 19326203 (ISSN)
Depositing User: مهندس مهدی شریفی
URI: http://eprints.medilam.ac.ir/id/eprint/1567

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