Wikidata

(Q50436280)

English

Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.

scientific article published on 19 October 2010

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Statements

title
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling. (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20937258
retrieved
14 March 2018
reference URL
http://europepmc.org/abstract/MED/20937258
author
Mustafa Tekin
object named as
Mustafa Tekin
series ordinal
5
0 references

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