A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance.
about
Mutation in BMPR2 Promoter: A 'Second Hit' for Manifestation of Pulmonary Arterial Hypertension?Treatment of monilethrix with oral minoxidil.Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.The hair follicle enigma.A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.Keratins: the hair shaft's backbone revealed.
P2860
A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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2012年學術文章
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name
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@en
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@nl
type
label
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@en
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@nl
prefLabel
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@en
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@nl
P2093
P2860
P1476
A novel monilethrix mutation i ...... ix with incomplete penetrance.
@en
P2093
P2860
P356
10.1111/J.1365-2133.2012.10861.X
P407
P478
166 Suppl 2
P577
2012-06-01T00:00:00Z