𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Is mucolipidosis type IV a neurodegenerative disorder?

✍ Scribed by Schiffmann, Raphael; Mayfield, Joan; Swift, Caren; Nestrasil, Igor

Book ID
122156019
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
70 KB
Volume
111
Category
Article
ISSN
1096-7192

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Chaperone-mediated autophagy is defectiv
Chaperone-mediated autophagy is defective in mucolipidosis type IV
✍ Bhuvarahamurthy Venugopal; Nicholas T. Mesires; John C. Kennedy; Cyntia Curcio-M πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 330 KB

## 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

92. A murine model for mucolipidosis typ
92. A murine model for mucolipidosis type IV
✍ Susan Slaugenhaupt; Cyntia Curcio-Morelli; Bhuvaramurthy Venugopal; Andrea Varro πŸ“‚ Article πŸ“… 2008 πŸ› Elsevier Science 🌐 English βš– 43 KB