Genetics of molybdenum cofactor deficiency

Human Genetics

Volumn 106, Issue 2, 2000, Pages 157-163

  Reiss, Jochen ^a,b  

^a Institut für Humangenetik   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE OXIDASE; MOLYBDENUM; MOLYBDENUM COFACTOR; MOLYBDENUM COMPLEX; SULFITE OXIDASE; SYNTHETASE; UNCLASSIFIED DRUG; XANTHINE DEHYDROGENASE;

AMINO ACID SEQUENCE; ANIMAL CELL; AUTOSOMAL RECESSIVE DISORDER; BIOSYNTHESIS; CARBOXY TERMINAL SEQUENCE; CISTRON; ENZYME DEFICIENCY; GENE EXPRESSION; GENE THERAPY; HUMAN; HUMAN CELL; MOLYBDENUM COFACTOR DEFICIENCY; NEUROLOGIC DISEASE; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; REVIEW; SEIZURE;

CARRIER PROTEINS; COENZYMES; DEFICIENCY DISEASES; GENE THERAPY; GENETIC COMPLEMENTATION TEST; HUMANS; MEMBRANE PROTEINS; METALLOPROTEINS; MOLECULAR SEQUENCE DATA; MOLYBDENUM; NUCLEAR PROTEINS; PTERIDINES; SULFURTRANSFERASES;

ANIMALIA;

EID: 0034058082     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051023     Document Type: Review

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