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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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Dettagli Bibliografici
Autori principali: Honey, N K, Mueller, O T, Little, L E, Miller, A L, Shows, T B
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1982
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC347351/
https://ncbi.nlm.nih.gov/pubmed/6961420
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