A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.
about
Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy.A Small Indel Mutant Mouse Model of Epidermolytic Palmoplantar Keratoderma and Its Application to Mutant-specific shRNA Therapy.The most common mutation of KRT9, c.C487T (p.R163W), in epidermolytic palmoplantar keratoderma in two large Chinese pedigrees.Analysis of the KRT9 gene in a Mexican family with epidermolytic palmoplantar keratoderma.
P2860
A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@en
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@nl
type
label
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@en
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@nl
prefLabel
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@en
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@nl
P2093
P2860
P1476
A novel mutation of keratin 9 ...... ytic palmoplantar keratoderma.
@en
P2093
P2860
P304
P356
10.1111/J.0007-0963.2004.05865.X
P407
P577
2004-04-01T00:00:00Z