KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr)

Tang MM 1 , Surana U 2 , Leong KF 3 , Pramano ZAD 4

Affiliations 

  • 1 Department of Dermatology, Hospital Kuala Lumpur, Ministry of Health Malaysia, Kuala Lumpur, Malaysia
  • 2 Institute of Molecular and Cellular Biology (IMCB), Agency of Science, Technology and Research (A*STAR), Singapore
  • 3 Paediatric Dermatology Unit, Women and Children Hospital, Ministry of Health Malaysia, Kuala Lumpur, Malaysia
  • 4 National Skin Centre, Singapore
Int J Dermatol, 2021 Jul;60(7):e288-e290.
PMID: 33728648 DOI: 10.1111/ijd.15523

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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