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

Tuysuz, Beyhan

Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation. [electronic resource] - JIMD reports 2016 - 7-12 p. digital

Publication Type: Journal Article

ISSN: 2192-8304

Standard No.: 10.1007/8904_2015_478 doi

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

APA

Tuysuz B., Pehlivan D., Özkök A., Jhangiani S., Yalcinkaya C., Zeybek Ç. A., Muzny D. M., Lupski J. R., Gibbs R. & Jaeken J. (20160512). Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation. : JIMD reports.

Chicago

Tuysuz Beyhan, Pehlivan Davut, Özkök Ahmet, Jhangiani Shalini, Yalcinkaya Cengiz, Zeybek Çiğdem Aktuğlu, Muzny Donna Marie, Lupski James R, Gibbs Richard and Jaeken Jaak. 20160512. Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation. : JIMD reports.

Harvard

Tuysuz B., Pehlivan D., Özkök A., Jhangiani S., Yalcinkaya C., Zeybek Ç. A., Muzny D. M., Lupski J. R., Gibbs R. and Jaeken J. (20160512). Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation. : JIMD reports.

MLA

Tuysuz Beyhan, Pehlivan Davut, Özkök Ahmet, Jhangiani Shalini, Yalcinkaya Cengiz, Zeybek Çiğdem Aktuğlu, Muzny Donna Marie, Lupski James R, Gibbs Richard and Jaeken Jaak. Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation. : JIMD reports. 20160512.

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