Familial Ectodermal Defect
نویسندگان
چکیده
منابع مشابه
Intra-familial variability of ectodermal defects associated with WNT10A mutations.
© 2011 The Authors. doi: 10.2340/00015555-1028 Journal Compilation © 2011 Acta Dermato-Venereologica. ISSN 0001-5555 WNT10A is a member of the wingless signalling pathway that has a fundamental role in skin and appendageal morphogenesis (1). Moreover, naturally occurring WNT10A gene mutations have been identified in the autosomal recessive human ectodermal dysplasia syndromes odonto-onycho-derm...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1937
ISSN: 0035-9157
DOI: 10.1177/003591573703100202