TY  - GEN
AU  - Christodoulou,J
AU  - McInnes,R R
AU  - Jay,V
AU  - Wilson,G
AU  - Becker,L E
AU  - Lehotay,D C
AU  - Platt,B A
AU  - Bridge,P J
AU  - Robinson,B H
AU  - Clarke,J T
TI  - Barth syndrome: clinical observations and genetic linkage studies
SN  - 0148-7299
PY  - 1994///0824
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Acids
KW  - urine
KW  - Cardiomyopathy, Dilated
KW  - Carnitine
KW  - metabolism
KW  - Diseases in Twins
KW  - Dwarfism
KW  - Electron Transport
KW  - Fasting
KW  - blood
KW  - Genes, Recessive
KW  - Genetic Linkage
KW  - Heart Failure
KW  - Hematopoiesis
KW  - Humans
KW  - Hypertrophy, Left Ventricular
KW  - Infant, Newborn
KW  - Male
KW  - Mitochondria, Muscle
KW  - enzymology
KW  - Mitochondrial Myopathies
KW  - Muscles
KW  - pathology
KW  - Neuromuscular Diseases
KW  - Neutropenia
KW  - Pedigree
KW  - Syndrome
KW  - X Chromosome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.1320500309
ER  -