TY  - GEN
AU  - Huizing,M
AU  - Wendel,U
AU  - Ruitenbeek,W
AU  - Iacobazzi,V
AU  - IJlst,L
AU  - Veenhuizen,P
AU  - Savelkoul,P
AU  - van den Heuvel,L P
AU  - Smeitink,J A
AU  - Wanders,R J
AU  - Trijbels,J M
AU  - Palmieri,F
TI  - Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient
SN  - 0141-8955
PY  - 1998///1104
KW  - Carnitine
KW  - metabolism
KW  - Carrier Proteins
KW  - genetics
KW  - Cells, Cultured
KW  - Fatty Acids
KW  - Female
KW  - Fibroblasts
KW  - Humans
KW  - Infant
KW  - Lipid Metabolism, Inborn Errors
KW  - Male
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1023/a:1005324323401
ER  -