Late-Infantile Neuronal Ceroid Lipfuscinosis

Source:http://linkedlifedata.com/resource/umls/id/C0022340

MSH: This type is caused by mutation in the CLN2 gene encoding tripeptidyl-peptidase I, a lysosomal serine protease.,NCI: Infantile neuronal ceroid lipofuscinosis in which the signs and symptoms appear later in life.

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