Title : Spermine synthase.

Pub. Date : 2010 Jan

PMID : 19859664






1 Functional Relationships(s)
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1 Mutations in the human SMS lead to a rise in spermidine and reduction of spermine causing Snyder-Robinson syndrome, an X-linked recessive condition characterized by mental retardation, skeletal defects, hypotonia, and movement disorders. Spermine spermine synthase Homo sapiens