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1 Ergebnisse
1
MYO5B,STX3, andSTXBP2mutations reveal a common disease mech..:
Dhekne, Herschel S.
;
Pylypenko, Olena
;
Overeem, Arend W.
...
Human Mutation. 39 (2018) 3 - p. 333-344 , 2018
Link:
https://doi.org/10.1002/humu.23386
RT Journal T1
MYO5B,STX3, andSTXBP2mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_humu.23386&Exemplar=1&LAN=DE A1 Dhekne, Herschel S. A1 Pylypenko, Olena A1 Overeem, Arend W. A1 Ferreira, Rosaria J. A1 van der Velde, K. Joeri A1 Rings, Edmond H.H.M. A1 Posovszky, Carsten A1 Swertz, Morris A. A1 Houdusse, Anne A1 van IJzendoorn, Sven C.D. PB Hindawi Limited YR 2018 SN 1059-7794 JF Human Mutation VO 39 IS 3 SP 333 OP 344 LK http://dx.doi.org/https://doi.org/10.1002/humu.23386 DO https://doi.org/10.1002/humu.23386 SF ELIB - SuUB Bremen
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