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Volumn 24, Issue 8, 2009, Pages 991-996
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Clinical heterogeneity in ethylmalonic encephalopathy.
a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ETHE1 PROTEIN, HUMAN;
MITOCHONDRIAL PROTEIN;
NUCLEOCYTOPLASMIC TRANSPORT PROTEIN;
ARTICLE;
BRAIN;
CASE REPORT;
CHILD;
DISEASE COURSE;
DNA SEQUENCE;
FEMALE;
GENETICS;
HUMAN;
INBORN ERROR OF METABOLISM;
MISSENSE MUTATION;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PATHOLOGY;
TWINS;
BRAIN;
CHILD;
DISEASE PROGRESSION;
DISEASES IN TWINS;
FEMALE;
HUMANS;
MAGNETIC RESONANCE IMAGING;
METABOLISM, INBORN ERRORS;
MITOCHONDRIAL PROTEINS;
MUTATION, MISSENSE;
NUCLEOCYTOPLASMIC TRANSPORT PROTEINS;
SEQUENCE ANALYSIS, DNA;
TWINS;
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EID: 70350717732
PISSN: None
EISSN: 17088283
Source Type: Journal
DOI: 10.1177/0883073808331359 Document Type: Article |
Times cited : (37)
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References (0)
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