author:"Gutiérrez Fernández, Ana Yolanda" | Pollux - Fachinformationsdienst Politikwissenschaft

Open Access#22013

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

This work has been supported by grants from Ministerio de Ciencia e Innovación-Spain, PCTI-FICYT Asturias, Fundación Centro Médico de Asturias, Fundación María Cristina Masaveu Peterson, and the European Union (FP7 Micro- EnviMet). C.L-O. is an investigator in the Botin Foundation. The Instituto Universitario de Oncología is supported by Obra Social Cajastur and Acción Transversal del Cáncer-RTICC

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Pleiotropic functions of the tumor- and metastasis-suppressing matrix metalloproteinase-8 in mammary cancer in MMTV-PyMT transgenic mice

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

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Pleiotropic functions of the tumor- and metastasis-suppressing matrix metalloproteinase-8 in mammary cancer in MMTV-PyMT transgenic mice

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

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