KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr)
2019 ◽
Vol 60
◽
pp. 164-166
◽
2010 ◽
Vol 52
(4)
◽
pp. e1-e4
◽
Keyword(s):
2006 ◽
Vol 29
(3)
◽
pp. 252-256
◽
2002 ◽
Vol 25
(2)
◽
pp. RC4-RC6
◽
Keyword(s):