Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case.
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M. Michaelides | M. Tesařová | T. Honzík | P. Lišková | V. Stránecký | H. Hansíková | N. Ondrušková | A. Čechová | B. Kousal | M. Meliska