Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

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Bibliographic Details
Published in:Journal of dermatological science 2010-06, Vol.58 (3), p.220-222
Main Authors: Nagy, Nikoletta, Wedgeworth, Emma, Hamada, Takahiro, White, Jonathan M, Hashimoto, Takashi, McGrath, John A
Format: Article
Language:English
Subjects:
Aged
Base Sequence
Codon, Nonsense
Dermatology
Ectodermal dysplasia
Ectodermal Dysplasia - genetics
Eyelid Diseases - genetics
Female
Hidrocystoma
Homozygote
Humans
Keratoderma, Palmoplantar - genetics
Nail Diseases - genetics
Syndrome
Wnt
Wnt Proteins - genetics
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ISSN:0923-1811
1873-569X
DOI:10.1016/j.jdermsci.2010.03.012