X-linked hypohidrotic ectodermal dysplasia (XLHED, OMIM 305100) is a rare congenital disorder that results in the defective development of teeth, hair, ...
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ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED; ECTD1 XLHED ECTODERMAL DYSPLASIA, ANHIDROTIC, X-LINKED; EDA EDA1 · Phenotype-Gene Relationships ...
19 авг. 2019 г. ... The molecular basis of X-linked hypohidrotic ectodermal dysplasia (XLHED) involves disruption in EDA protein [1]. The EDA protein is a type II ...
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Based on the family history and clinical information, a single nucleotide variant in the EDA gene was suspected to be the cause of possible X-linked ...
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1 июн. 2001 г. ... Mutations in the epithelial morphogen ectodysplasin-A (EDA), a member of the tumor necrosis factor (TNF) family, are responsible for the ...
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