A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
about
Congenital hair loss disorders: rare, but not too rare.Epidermal barrier disorders and corneodesmosome defects.Inherited desmosomal disorders.Regulation of mitotic spindle orientation during epidermal stratification.Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B.Alu-mediated large deletion of the CDSN gene as a cause of peeling skin disease.A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.Inflammatory peeling skin syndrome caused a novel mutation in CDSN.
P2860
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P2860
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年學術文章
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2010年學術文章
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name
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@en
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@nl
type
label
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@en
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@nl
prefLabel
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@en
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin.
@nl
P2093
P50
P356
P1433
P1476
A new amyloidosis caused by fibrillar aggregates of mutated corneodesmosin
@en
P2093
Cécile Caubet
Fanny Coudane
Luc Bousset
Ole Clemmensen
Regina C Betz
Ronald Melki
Yannick Sourigues
P304
P356
10.1096/FJ.10-155622
P407
P577
2010-05-06T00:00:00Z