Title : Infantile neuronal ceroid lipofuscinosis: no longer just a 'Finnish' disease.

Pub. Date : 2001

PMID : 11589007






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The most severe (infantile) form of NCL is caused by mutations in a lysosomal thioesterase that removes fatty acids from modified cysteine residues in proteins. Cysteine nucleolin Homo sapiens