Gene symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency

Human Genetics

Volumn 113, Issue 4, 2003, Pages 365-

  Hwu, Wuh Liang ^a   Huang, Yuan Te ^a   Chien, Yin Hsiu ^a   Yeh, Hui Ying ^a   Lul, Frank ^a   Chou, Shi Ping ^a   Lin, Jing Meei ^a   Chiang, Shu Chuan ^a  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ORNITHINE CARBAMOYLTRANSFERASE; ASPARAGINE; ORNITHINE DECARBOXYLASE; THREONINE;

CODON; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; GENE DELETION; GENE SEQUENCE; HUMAN; NOTE; PRIORITY JOURNAL; AMINO ACID SUBSTITUTION; BASE PAIRING; MISSENSE MUTATION; NONSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; ARTICLE; GENETICS; NOMENCLATURE;

AMINO ACID SUBSTITUTION; HUMANS; MUTATION, MISSENSE; ORNITHINE CARBAMOYLTRANSFERASE; ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY DISEASE; TERMINOLOGY;

EID: 0141765867     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-003-0994-5     Document Type: Note

References (0)