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Volumn 98, Issue 3, 2009, Pages 553-554
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Abnormal growth in mitochondrial disease
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Author keywords
Growth; Mitochondrial diseases; Short stature
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Indexed keywords
PYRUVATE DEHYDROGENASE;
ADOLESCENT;
ADULT;
ARTICLE;
AUTOSOMAL DOMINANT OPTIC ATROPHY;
BODY HEIGHT;
BODY MASS;
CHILD;
COMPLEX I DEFICIENCY;
COMPLEX II DEFICIENCY;
COMPLEX III DEFICIENCY;
CONFIDENCE INTERVAL;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
ENZYME DEFICIENCY;
FEMALE;
GENE DELETION;
GROWTH;
HUMAN;
KEARNS SAYRE SYNDROME;
LEIGH DISEASE;
MAJOR CLINICAL STUDY;
MALE;
MEDICAL AUDIT;
MELAS SYNDROME;
PEARSON SYNDROME;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
SCHOOL CHILD;
SHORT STATURE;
UNITED KINGDOM;
WEIGHT;
ADOLESCENT;
ADOLESCENT DEVELOPMENT;
BODY HEIGHT;
BODY WEIGHT;
CHILD;
CHILD DEVELOPMENT;
CHILD, PRESCHOOL;
CROSS-SECTIONAL STUDIES;
HUMANS;
INFANT;
MITOCHONDRIAL DISEASES;
RETROSPECTIVE STUDIES;
YOUNG ADULT;
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EID: 59149103480
PISSN: 08035253
EISSN: 16512227
Source Type: Journal
DOI: 10.1111/j.1651-2227.2008.01148.x Document Type: Article |
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Times cited : (36)
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References (5)
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