Large case-control study and functional analyses show that FANCM truncating mutations are associated with a breast cancer risk magnitude that varies depending on their location

doi:10.1038/s41431-019-0404-7

Large case-control study and functional analyses show that FANCM truncating mutations are associated with a breast cancer risk magnitude that varies depending on their location

Departamento de Genética y Microbiología

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

Idioma original	Inglés
Páginas (desde-hasta)	405-406
Número de páginas	2
Publicación	European Journal of Human Genetics
Volumen	27
N.º	s1
DOI	https://doi.org/10.1038/s41431-019-0404-7
Estado	Publicada - jul 2019

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

Acceder al documento

10.1038/s41431-019-0404-7

Otros archivos y enlaces

Ver registro en Web of Science

Citar esto

@article{c673f203e4944894af49285a42d94dbc,

title = "Large case-control study and functional analyses show that FANCM truncating mutations are associated with a breast cancer risk magnitude that varies depending on their location",

author = "G. Figlioli and M. Bogliolo and L. Caleca and P. Radice and J. Surralles and P. Peterlongo",

year = "2019",

month = jul,

doi = "10.1038/s41431-019-0404-7",

language = "English",

volume = "27",

pages = "405--406",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

number = "s1",

}

TY - JOUR

T1 - Large case-control study and functional analyses show that FANCM truncating mutations are associated with a breast cancer risk magnitude that varies depending on their location

AU - Figlioli, G.

AU - Bogliolo, M.

AU - Caleca, L.

AU - Radice, P.

AU - Surralles, J.

AU - Peterlongo, P.

PY - 2019/7

Y1 - 2019/7

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=uab_pure&SrcAuth=WosAPI&KeyUT=WOS:000489313103161&DestLinkType=FullRecord&DestApp=WOS

U2 - 10.1038/s41431-019-0404-7

DO - 10.1038/s41431-019-0404-7

M3 - Article

SN - 1018-4813

VL - 27

SP - 405

EP - 406

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - s1

ER -