Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas-Reference-Cited by-同舟云学术

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

Published:2019-04 Issue:4 Volume:104 Page:651-664
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Remacha Laura,Pirman David,Mahoney Christopher E.,Coloma Javier,Calsina Bruna,Currás-Freixes Maria,Letón Rocío,Torres-Pérez Rafael,Richter Susan,Pita Guillermo,Herráez Belén,Cianchetta Giovanni,Honrado Emiliano,Maestre Lorena,Urioste Miguel,Aller Javier,García-Uriarte Óscar,Gálvez María Ángeles,Luque Raúl M.,Lahera Marcos,Moreno-Rengel Cristina,Eisenhofer Graeme,Montero-Conde Cristina,Rodríguez-Antona Cristina,Llorca Óscar,Smolen Gromoslaw A.,Robledo Mercedes,Cascón Alberto

Funder

Instituto de Salud Carlos III

European Regional Development Fund

Deutsche Forschungsgemeinschaft

ISCIII

ERDF

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference57 articles.

1. Consensus statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas;Toledo;Nat. Rev. Endocrinol.,2017