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111. Autophagic dysfunction in mucolipidosis type IV patients

✍ Scribed by Rosa Puertollano; Silvia Vergarajauregui; Jose Martina


Book ID
116988545
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
42 KB
Volume
96
Category
Article
ISSN
1096-7192

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## Abstract Mucolipidosis type IV (MLIV) is a lysosomal storage disorder caused by mutations in the __MCOLN1__ gene, a member of the transient receptor potential (TRP) cation channel gene family. The encoded protein, transient receptor potential mucolipin‐1 (TRPML1), has been localized to lysosomes