Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
about
Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.A novel dominant GJB2 (DFNA3) mutation in a Chinese family.Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26.EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus.
P2860
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年學術文章
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2011年學術文章
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2011年學術文章
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name
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@en
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@nl
type
label
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@en
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@nl
prefLabel
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@en
Two Iranian families with a no ...... ant nonsyndromic hearing loss.
@nl
P2093
P2860
P50
P356
P1476
Two Iranian families with a no ...... nant nonsyndromic hearing loss
@en
P2093
Abraham M Sheffield
Carla Nishimura
Farkhondeh Habibi
Masoomeh Sobhani
Matthew R Avenarius
Nele Hilgert
Nicole C Meyer
Niloofar Bazazzadegan
Seyedeh Sedigheh Abedini
P2860
P304
P356
10.1002/AJMG.A.33209
P407
P577
2011-04-11T00:00:00Z