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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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Detaylı Bibliyografya
Asıl Yazarlar: Venkatachalam, Kartik, Hofmann, Thomas, Montell, Craig
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2006
Konular:
Online Erişim: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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