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An intronic variation in SLC52A1 causes exon skipping and t..:
Mosegaard, Signe
;
Bruun, Gitte Hoffmann
;
Flyvbjerg, Karen Freund
...
Molecular Genetics and Metabolism. 122 (2017) 4 - p. 182-188 , 2017
Link:
https://doi.org/10.1016/j.ymgme.2017.10.014
RT Journal T1
An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ymgme.2017.10.014&Exemplar=1&LAN=DE A1 Mosegaard, Signe A1 Bruun, Gitte Hoffmann A1 Flyvbjerg, Karen Freund A1 Bliksrud, Yngve Thomas A1 Gregersen, Niels A1 Dembic, Maja A1 Annexstad, Ellen A1 Tangeraas, Trine A1 Olsen, Rikke Katrine Jentoft A1 Andresen, Brage S. PB Elsevier BV YR 2017 SN 1096-7192 JF Molecular Genetics and Metabolism VO 122 IS 4 SP 182 OP 188 LK http://dx.doi.org/https://doi.org/10.1016/j.ymgme.2017.10.014 DO https://doi.org/10.1016/j.ymgme.2017.10.014 SF ELIB - SuUB Bremen
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