Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population

Journal name: Journal of human genetics / Japan Society of Human Genetics 58(2):2013.2

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Material Type: 記事
Title: Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population
Author/Editor: Zil-e-Huma Bashir
Noreen Latief
Inna A Belyantseva 他
Author Heading: Zil-e-Huma Bashir
Noreen Latief
Inna A Belyantseva
Periodical title: Journal of human genetics / Japan Society of Human Genetics
No. or year of volume/issue: 58(2):2013.2
Volume: 58
Issue: 2
Pages: 102-108
Publication date of volume/issue (W3CDTF): 2013-02
ISSN (Periodical Title): 1434-5161
Publication (Periodical Title): Tokyo : Springer Nature
Place of Publication (Country Code): JP
Text Language Code: eng
Subject Heading: CLDN14
claudin 14
DFNB29
mild hearing loss
Pakistan
profound deafness
NDLC: ZS16
Target Audience: 一般
Holding library: 国立国会図書館
Call No.: Z54-H248
Data Provider (Database): 国立国会図書館 : 国立国会図書館雑誌記事索引
https://ndlsearch.ndl.go.jp
Bibliographic ID (NDL): 024272421
http://id.ndl.go.jp/bib/024272421
Bibliographic Record Category (NDL): 632