A novel mutation in the succinate dehydrogenase subunit D gene in siblings with the hereditary paraganglioma–pheochromocytoma syndrome

Germline mutations in the succinate dehydrogenase complex subunit D gene are now known to be associated with hereditary paraganglioma–pheochromocytoma syndromes. Since the initial succinate dehydrogenase complex subunit D gene mutation was identified about a decade ago, more than 131 unique variants...

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Detalles Bibliográficos
Autores principales: Prasad, Chaithra, Oakley, Gerard J, Yip, Linwah, Coyne, Christopher, Rangaswamy, Balasubramanya, Dixit, Sanjay B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857366/
https://www.ncbi.nlm.nih.gov/pubmed/27489656
http://dx.doi.org/10.1177/2050313X14553520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857366/
https://www.ncbi.nlm.nih.gov/pubmed/27489656
http://dx.doi.org/10.1177/2050313X14553520

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