Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis

Recent genetic studies yielded conflicting results regarding a role for the variant chromogranin B (CHGB)(P413L) allele as a disease modifier in ALS. Moreover, potential deleterious effects of the CHGB(P413L) variant in ALS pathology have not been investigated. Here we report that in transfected cul...

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Xehetasun bibliografikoak
Argitaratua izan da:Hum Mol Genet
Egile Nagusiak: Ohta, Yasuyuki, Soucy, Genevieve, Phaneuf, Daniel, Audet, Jean-Nicolas, Gros-Louis, François, Rouleau, Guy A., Blasco, Hélène, Corcia, Philippe, Andersen, Peter M., Nordin, Frida, Yamashita, Toru, Abe, Koji, Julien, Jean-Pierre
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2016
Gaiak:
Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5418737/
https://ncbi.nlm.nih.gov/pubmed/28175304
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw304
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