Title : Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography.

Pub. Date : 1978 Dec

PMID : 282632






1 Functional Relationships(s)
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1 Argininosuccinic aciduria, an autosomal recessive disorder of the urea cycle in humans, is associated with a deficiency of argininosuccinate lyase (ASL; L-argininosuccinate arginine-lyase, EC 4.3.2.1). Urea argininosuccinate lyase Homo sapiens