Mucolipidosis III is genetically heterogeneous.

Mucolipidosis III (ML III), or pseudo-Hurler polydystrophy, is an inherited childhood disorder characterized biochemically by low activities and abnormal electrophoretic patterns of multiple lysosomal enzymes in fibroblasts. The primary deficiency of ML III has been proposed to be in UDP-N-acetylglu...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Honey, N K, Mueller, O T, Little, L E, Miller, A L, Shows, T B
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 1982
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC347351/
https://ncbi.nlm.nih.gov/pubmed/6961420
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