The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

Asli Sirmaci; Duygu Akcayoz-Duman; Mustafa Tekin

doi:10.1007/BF02935334

The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

Asli Sirmaci, Duygu Akcayoz-Duman, Mustafa Tekin

Hussman Institute for Human Genomics

Research output: Contribution to journal › Article

38 Scopus citations

Original language	English (US)
Pages (from-to)	213-216
Number of pages	4
Journal	Journal of Genetics
Volume	85
Issue number	3
DOIs	https://doi.org/10.1007/BF02935334
State	Published - Dec 1 2006

Keywords

Connexin26
Connexin30
Deafness
Gap junctions
GJB2
GJB6
Hearing impairment

ASJC Scopus subject areas

Genetics

Cite this

Sirmaci, A., Akcayoz-Duman, D., & Tekin, M. (2006). The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population. Journal of Genetics, 85(3), 213-216. https://doi.org/10.1007/BF02935334

@article{e978b60111694e22a7de9283aac194c6,

title = "The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population",

keywords = "Connexin26, Connexin30, Deafness, Gap junctions, GJB2, GJB6, Hearing impairment",

author = "Asli Sirmaci and Duygu Akcayoz-Duman and Mustafa Tekin",

year = "2006",

month = dec

day = "1",

doi = "10.1007/BF02935334",

language = "English (US)",

volume = "85",

pages = "213--216",

journal = "Journal of Genetics",

issn = "0022-1333",

publisher = "Springer India",

number = "3",

}

TY - JOUR

T1 - The c.IVS1+1G>A mutation inthe GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population

AU - Sirmaci, Asli

AU - Akcayoz-Duman, Duygu

AU - Tekin, Mustafa

PY - 2006/12/1

Y1 - 2006/12/1

KW - Connexin26

KW - Connexin30

KW - Deafness

KW - Gap junctions

KW - GJB2

KW - GJB6

KW - Hearing impairment

UR - http://www.scopus.com/inward/record.url?scp=33947640972&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33947640972&partnerID=8YFLogxK

U2 - 10.1007/BF02935334

DO - 10.1007/BF02935334

M3 - Article

C2 - 17406097

AN - SCOPUS:33947640972

VL - 85

SP - 213

EP - 216

JO - Journal of Genetics

JF - Journal of Genetics

SN - 0022-1333

IS - 3

ER -

Access to Document

10.1007/BF02935334