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Volumn 30, Issue 2, 2002, Pages 145-146
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Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation
a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
MITOCHONDRIAL DNA;
TRANSFER RNA;
ADULT;
ARTICLE;
CLINICAL ARTICLE;
FEMALE;
GENE MUTATION;
GENETIC ANALYSIS;
GENETIC DISORDER;
HUMAN;
LEIGH DISEASE;
MALE;
MULTIGENE FAMILY;
NEWBORN;
NEWBORN MORTALITY;
PATHOGENESIS;
PEDIGREE;
PHENOTYPE;
PRIORITY JOURNAL;
ADULT;
DNA MUTATIONAL ANALYSIS;
DNA, MITOCHONDRIAL;
FEMALE;
HUMANS;
INFANT, NEWBORN;
LEIGH DISEASE;
MALE;
MITOCHONDRIAL DISEASES;
MUTATION;
PEDIGREE;
PHENOTYPE;
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EID: 0036478952
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/ng819 Document Type: Article |
Times cited : (149)
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References (14)
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