Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.

Author
PEHLIVAN, Davut
ZEYBEK, ÇA
JHANGIANI, S
Tuysuz, Beyhan
YALCINKAYA, Cengiz
MUZNY, DM
LUPSKI, JR
GIBBS, R
JAEKEN, J
ÖZKÖK, A
Metadata
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URI
http://hdl.handle.net/20.500.12627/85017
https://doi.org/10.1007/8904_2015_478
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