A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL

BACKGROUND: More than 40% of patients with paragangliomas (PGLs) harbor a germline mutation of the known PGL susceptibility genes, mainly in the SDHB or SDHD genes. OBJECTIVE: The objective of the study was to characterize the genetic background of the French Canadian (FC) patients with PGLs and pro...

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Vydáno v:J Clin Endocrinol Metab
Hlavní autoři: Bourdeau, Isabelle, Grunenwald, Solange, Burnichon, Nelly, Khalifa, Emmanuel, Dumas, Nadine, Binet, Marie-Claire, Nolet, Serge, Gimenez-Roqueplo, Anne-Paule
Médium: Artigo
Jazyk:Inglês
Vydáno: Endocrine Society 2016
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5155677/
https://ncbi.nlm.nih.gov/pubmed/27700540
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2016-1665
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