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Volumn 52, Issue 1, 2002, Pages 95-99
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Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
ADENINE NUCLEOTIDE TRANSLOCASE;
UNCLASSIFIED DRUG;
ADOLESCENT;
ADULT;
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
CONGENITAL CATARACT;
DISEASE ASSOCIATION;
GENETIC DISORDER;
GENETIC TRANSCRIPTION;
HUMAN;
HUMAN TISSUE;
HYPERTROPHIC CARDIOMYOPATHY;
LACTIC ACIDOSIS;
LINKAGE ANALYSIS;
MALE;
MITOCHONDRIAL MYOPATHY;
MUSCLE LEVEL;
OXIDATION;
PRIORITY JOURNAL;
PROTEIN FUNCTION;
PROTEIN PROCESSING;
RNA TRANSLATION;
SENGERS SYNDROME;
SEQUENCE ANALYSIS;
SYMPTOM;
SYNDROME;
BIOLOGICAL TRANSPORT;
FEMALE;
HUMANS;
LINKAGE (GENETICS);
MALE;
MITOCHONDRIA, HEART;
MITOCHONDRIAL ADP, ATP TRANSLOCASES;
MITOCHONDRIAL MYOPATHIES;
MYOCARDIUM;
PEDIGREE;
SYNDROME;
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EID: 0036288502
PISSN: 03645134
EISSN: None
Source Type: Journal
DOI: 10.1002/ana.10214 Document Type: Article |
Times cited : (76)
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References (17)
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