Mutation inKANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference40 articles.
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3. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma;Norgett;Hum Mol Genet,2000
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