TY  - GEN
AU  - Bennett,M J
AU  - Hale,D E
AU  - Pollitt,R J
AU  - Stanley,C A
AU  - Variend,S
TI  - Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter
SN  - 0160-9289
PY  - 1996///0809
KW  - Cardiomyopathy, Dilated
KW  - etiology
KW  - Carnitine
KW  - deficiency
KW  - Cell Membrane
KW  - metabolism
KW  - Endocardial Fibroelastosis
KW  - Female
KW  - Fibroblasts
KW  - Genetic Carrier Screening
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Ion Channels
KW  - genetics
KW  - Ion Transport
KW  - Liver
KW  - Metabolism, Inborn Errors
KW  - complications
KW  - Muscle, Skeletal
KW  - Myocardium
KW  - Skin
N1  - Publication Type: Case Reports; Clinical Conference; Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/clc.4960190320
ER  -