The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population

Letter/Communication

N Mahdieh, C Nishimura, K Ali-Madadi, Y Riazalhosseini, H Yazdan, S Arzhangi, K Jalalvand, A Ebrahimi, S Kazemi, R J H Smith, …

Clinical genetics, Vol.65(6), pp.506-508

06/2004

DOI: 10.1111/j.1399-0004.2004.00262.x

PMID: 15151513

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Letter to the editor

Mutation

Connexin 26

Hearing Loss - genetics

Gene Frequency - genetics

Ethnic Groups - genetics

Hearing Loss - ethnology

Humans

Connexins - genetics

Sequence Deletion - genetics

Title: Subtitle: The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population
Creators: N Mahdieh
C Nishimura
K Ali-Madadi
Y Riazalhosseini
H Yazdan
S Arzhangi
K Jalalvand
A Ebrahimi
S Kazemi
R J H Smith
H Najmabadi
Resource Type: Letter/Communication
Publication Details: Clinical genetics, Vol.65(6), pp.506-508
DOI: 10.1111/j.1399-0004.2004.00262.x
PMID: 15151513
NLM abbreviation: Clin Genet
ISSN: 0009-9163
eISSN: 1399-0004
Publisher: Denmark
Grant note: R01 02842 / PHS HHS
Language: English
Date published: 06/2004
Academic Unit: Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
Record Identifier: 9984007186402771

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