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...

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Bibliografische gegevens
Hoofdauteurs: Honey, N K, Mueller, O T, Little, L E, Miller, A L, Shows, T B
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1982
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC347351/
https://ncbi.nlm.nih.gov/pubmed/6961420
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