María
Currás Freixes
Investigadora ata 2022
Complejo Asistencial Universitario de León
León, EspañaPublicacións en colaboración con investigadores/as de Complejo Asistencial Universitario de León (3)
2018
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Gain-of-function mutations in DNMT3A in patients with paraganglioma
Genetics in Medicine, Vol. 20, Núm. 12, pp. 1644-1651
2017
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Targeted exome sequencing of Krebs cycle genes reveals candidate cancer–predisposing mutations in pheochromocytomas and paragangliomas
Clinical Cancer Research, Vol. 23, Núm. 20, pp. 6315-6325
2015
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Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients
Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656