Načítá se...

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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Venkatachalam, Kartik, Hofmann, Thomas, Montell, Craig
Médium: Artigo
Jazyk:Inglês
Vydáno: 2006
Témata:
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!