A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
about
Epidermal barrier disorders and corneodesmosome defects.A Case of Inflammatory Generalized Type of Peeling Skin Syndrome Possibly Caused by a Homozygous Missense Mutation of CDSN.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.Inflammatory peeling skin syndrome caused by homozygous genomic deletion in thePSORS1region encompassing theCDSNgene
P2860
A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
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2011 nî lūn-bûn
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A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
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A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
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A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
@en
A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
@nl
prefLabel
A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
@en
A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
@nl
P2093
P2860
P1476
A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
@en
P2093
E A Leclerc
J Mazereeuw-Hautier
P2860
P304
P356
10.1111/J.1365-2133.2011.10529.X
P407
P577
2011-11-01T00:00:00Z