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Volumn 59, Issue 11, 2001, Pages 2278-2284
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Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)
a
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID TRANSPORTER;
AMMONIA;
CARRIER PROTEIN;
CITRULLINE;
ORNITHINE;
ORNITHINE TRANSPORTER;
SLC25A2 PROTEIN, HUMAN;
ANIMAL;
BLOOD;
GENETICS;
HUMAN;
MITOCHONDRION;
MOLECULAR GENETICS;
MUTATION;
NEUROLOGIC DISEASE;
NUCLEOTIDE SEQUENCE;
REVIEW;
SYNDROME;
URINE;
AMINO ACID TRANSPORT SYSTEMS, BASIC;
AMMONIA;
ANIMALS;
BASE SEQUENCE;
CARRIER PROTEINS;
CITRULLINE;
HUMANS;
MEMBRANE TRANSPORT PROTEINS;
MITOCHONDRIA;
MOLECULAR SEQUENCE DATA;
MUTATION;
NERVOUS SYSTEM DISEASES;
ORNITHINE;
SYNDROME;
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EID: 0035512274
PISSN: 00471852
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (2)
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References (20)
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