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Lysosomal deficiencies and cell death in mucolipidosis type IV

✍ Scribed by G. Colletti; Y. Rbaibi; M. Meidel; J. Jennings; O. A. Weisz; K. I. Kiselyov


Book ID
111471815
Publisher
SP MAIK Nauka/Interperiodica
Year
2009
Tongue
English
Weight
74 KB
Volume
3
Category
Article
ISSN
1990-7478

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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