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...

Descrizione completa

Salvato in:
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
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC347351/
https://ncbi.nlm.nih.gov/pubmed/6961420
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi