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A mutation creating an upstream translation initiation codo..:
Ferdinandusse, Sacha
;
te Brinke, Heleen
;
Ruiter, Jos P.N.
...
Human Mutation. 40 (2019) 10 - p. 1899-1904 , 2019
Link:
https://doi.org/10.1002/humu.23839
RT Journal T1
A mutation creating an upstream translation initiation codon inSLC22A55′UTR is a frequent cause of primary carnitine deficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_humu.23839&Exemplar=1&LAN=DE A1 Ferdinandusse, Sacha A1 te Brinke, Heleen A1 Ruiter, Jos P.N. A1 Haasjes, Janet A1 Oostheim, Wendy A1 Lenthe, Henk A1 IJlst, Lodewijk A1 Ebberink, Merel S. A1 Wanders, Ronald J.A. A1 Vaz, Frédéric M. A1 Waterham, Hans R. PB Hindawi Limited YR 2019 SN 1059-7794 SN 1098-1004 JF Human Mutation VO 40 IS 10 SP 1899 OP 1904 LK http://dx.doi.org/https://doi.org/10.1002/humu.23839 DO https://doi.org/10.1002/humu.23839 SF ELIB - SuUB Bremen
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