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A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large
ISSN号:0007-0963
期刊名称:British Journal of Dermatology
时间:2012.10
页码:952-954
相关项目:马拉色菌及其变应原致敏FLG突变小鼠的机制
作者:
Li M|Cheng R|Zhuang Y|Yao Z|
同期刊论文项目
马拉色菌及其变应原致敏FLG突变小鼠的机制
期刊论文 16
同项目期刊论文
Interactions between FLG mutations and allergens in atopic dermatitis.
Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis
Genotype-phenotype correlation of xeroderma pigmentosum in a Chinese Han population.
Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos diseas
Gene diagnosis and prenatal genetic diagnosis of a case of dystrophic epidermolysis bullosa family c
Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis.
Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a
Prevalent and rare mutations in IL-36RN gene in Chinese patients with generalized pustular psoriasis
A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa prurigino
Analyses of FLG mutation frequency and filaggrin expression in isolatedichthyosis vulgaris (IV) and
Common FLG mutation K4671X not associated with atopic dermatitis in Han Chinese in a family associat
Lidocaine inhibits staphylococcal enterotoxin-stimulated activation of peripheral blood mononuclear
Effects of lidocaine on regulatory T cells in atopic dermatitis.