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Isolated glycerol kinase deficiency in a neonate
B. Lewis
, M. Harbord
, R. Keenan
, W. Carey
, R. Harrison
, E. Robertson
Research output
:
Contribution to journal
›
Article
›
peer-review
11
Citations (Scopus)
Overview
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Pharmacology, Toxicology and Pharmaceutical Science
Glycerol Kinase
100%
Syndrome
66%
Apnea
66%
Developmental Delay
66%
Muscle Hypotonia
66%
Communicating Hydrocephalus
33%
Enzyme Deficiency
33%
Enzyme Defect
33%
Duchenne Muscular Dystrophy
33%
Myopathy
33%
Adrenal Insufficiency
33%
Hypoplasia
33%
Neuroscience
Glycerol Kinase
100%
Enzymes
66%
Hypotonia
66%
Magnetic Resonance Imaging
33%
Muscle Disorder
33%
Muscular Dystrophy
33%
Hydrocephalus
33%
X Chromosome
33%
Hypoplasia
33%
Adrenal Insufficiency
33%
Biochemistry, Genetics and Molecular Biology
Glycerol Kinase Deficiency
100%
Enzyme
66%
Magnetic Resonance Imaging
33%
X Chromosome
33%
Microdeletion Syndrome
33%
P21
33%
Deficiency
33%