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KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr).
Min-Moon Tang
Uttam Surana
Kin F Leong
Zacharias Aloysius Dwi Pramano
Published in:
International journal of dermatology (2021)
Keyphrases
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early onset
mental health
intellectual disability
case report
hearing loss
bioinformatics analysis