Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus.

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Bibliographic Details
Title: Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus.
Authors: Chan JCK; Department of Clinical Genetics, Hong Kong Children's Hospital, Hong Kong, China., Siu LLP, Ho SKL, Cheng SSW, Luk HM
Source: Clinical dysmorphology [Clin Dysmorphol] 2025 Oct 01; Vol. 34 (4), pp. 142-146. Date of Electronic Publication: 2025 Jun 30.
Publication Type: Journal Article
Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
Description
ISSN:1473-5717
DOI:10.1097/MCD.0000000000000531