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Volumn 128, Issue 15, 2012, Pages 1560-1567
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[GRACILE syndrome--a severe neonatal mitochondrial disorder].;SGRACILE-oireyhtymä--vastasyntyneen vakava mitokondriotauti.
a
a
Lundin
(United States)
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Author keywords
[No Author keywords available]
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Indexed keywords
BCS1L PROTEIN, HUMAN;
BIOLOGICAL MARKER;
UBIQUINOL CYTOCHROME C REDUCTASE;
AMINOACIDURIA;
BLOOD;
CHOLESTASIS;
FINLAND;
GENETICS;
HEMOSIDEROSIS;
HUMAN;
INBORN ERROR OF METABOLISM;
INTRAUTERINE GROWTH RETARDATION;
LACTIC ACIDOSIS;
NEWBORN;
POINT MUTATION;
REVIEW;
ACIDOSIS, LACTIC;
BIOLOGICAL MARKERS;
CHOLESTASIS;
ELECTRON TRANSPORT COMPLEX III;
FETAL GROWTH RETARDATION;
FINLAND;
HEMOSIDEROSIS;
HUMANS;
INFANT, NEWBORN;
METABOLISM, INBORN ERRORS;
POINT MUTATION;
RENAL AMINOACIDURIAS;
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EID: 84867908668
PISSN: 00127183
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (4)
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References (0)
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