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Phenotypic severity of homozygous GCK mutations causing neo..:
Raimondo, Anne
;
Chakera, Ali J.
;
Thomsen, Soren K.
...
Human Molecular Genetics. 23 (2014) 24 - p. 6432-6440 , 2014
Link:
https://doi.org/10.1093/hmg/ddu360
RT Journal T1
Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddu360&Exemplar=1&LAN=DE A1 Raimondo, Anne A1 Chakera, Ali J. A1 Thomsen, Soren K. A1 Colclough, Kevin A1 Barrett, Amy A1 De Franco, Elisa A1 Chatelas, Alisson A1 Demirbilek, Huseyin A1 Akcay, Teoman A1 Alawneh, Hussein A1 Flanagan, Sarah E. A1 Van De Bunt, Martijn A1 Hattersley, Andrew T. A1 Gloyn, Anna L. A1 Ellard, Sian A1 Abduljabbar, Mohammad A. A1 Al-Zyoud, Mahmoud A1 Aman, Syed A1 Bath, Louise A1 De, Parijat A1 Deshpande, Neeta A1 Durmaz, Erdem A1 Eickmeier, Frank A1 Elbarbary, Nancy Samir A1 Fillion, Marc A1 Jagadeesh, Sujatha M. A1 Kershaw, Melanie A1 Khan, Waqas I. A1 Mlynarski, Wojciech A1 Noyes, Kathryn PB Oxford University Press (OUP) YR 2014 SN 1460-2083 SN 0964-6906 JF Human Molecular Genetics VO 23 IS 24 SP 6432 OP 6440 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddu360 DO https://doi.org/10.1093/hmg/ddu360 SF ELIB - SuUB Bremen
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