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Lysosomal Localization of TRPML3 Depends on TRPML2 and the Mucolipidosis-associated Protein TRPML1

Mucolipidosis type IV is an autosomal recessive lysosomal storage disorder characterized by severe neurodegeneration, achlorhydria, and visual impairments such as corneal opacity and strabismus. The disease arises due to mutations in a group 2 transient receptor potential (TRP)-related cation channe...

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Autors principals: Venkatachalam, Kartik, Hofmann, Thomas, Montell, Craig
Format: Artigo
Idioma:Inglês
Publicat: 2006
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4196876/
https://ncbi.nlm.nih.gov/pubmed/16606612
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M600807200
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