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A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain()

Mutations in the eye lens gap junction protein connexin 50 cause cataract. Earlier we identified a frameshift mutant of connexin 50 (c.670insA; p.Thr203AsnfsX47) in a family with autosomal recessive cataract. The mutant protein is smaller and contains 46 aberrant amino acids at the C-terminus after...

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Библиографические подробности
Главные авторы: Somaraju Chalasani, Madhavi Latha, Muppirala, Madhavi, G. Ponnam, Surya Prakash, Kannabiran, Chitra, Swarup, Ghanshyam
Формат: Artigo
Язык:Inglês
Опубликовано: Elsevier 2012
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3668514/
https://ncbi.nlm.nih.gov/pubmed/23772370
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fob.2012.11.005
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