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  1. KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr)
    Tang MM, Surana U, Leong KF, Pramano ZAD
    Int J Dermatol, 2021 Jul;60(7):e288-e290.
    PMID: 33728648 DOI: 10.1111/ijd.15523
  2. H syndrome - the first report in Malaysia
    Low DE, Tang MM, Surana U, Lee JY, Pramano ZAD, Leong KF
    Int J Dermatol, 2019 Oct;58(10):e190-e193.
    PMID: 31192449 DOI: 10.1111/ijd.14518
  3. CHILD syndrome in a Malaysian adult with identification of a novel heterozygous missense mutation NSDHL c.602A>G
    Tang MM, Tan WC, Surana U, Leong KF, Pramano ZAD
    Int J Dermatol, 2021 Apr;60(4):e154-e156.
    PMID: 33169834 DOI: 10.1111/ijd.15296
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