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Functional characterization of a humanPOU1F1mutation associ..:
Sobrier, Marie-Laure
;
Tsai, Yu-Cheng
;
Pérez, Christelle
...
Human Molecular Genetics. 25 (2015) 3 - p. 472-483 , 2015
Link:
https://doi.org/10.1093/hmg/ddv486
RT Journal T1
Functional characterization of a humanPOU1F1mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddv486&Exemplar=1&LAN=DE A1 Sobrier, Marie-Laure A1 Tsai, Yu-Cheng A1 Pérez, Christelle A1 Leheup, Bruno A1 Bouceba, Tahar A1 Duquesnoy, Philippe A1 Copin, Bruno A1 Sizova, Daria A1 Penzo, Alfredo A1 Stanger, Ben Z. A1 Cooke, Nancy E. A1 Liebhaber, Stephen A. A1 Amselem, Serge PB Oxford University Press (OUP) YR 2015 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 25 IS 3 SP 472 OP 483 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddv486 DO https://doi.org/10.1093/hmg/ddv486 SF ELIB - SuUB Bremen
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