Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome
- Puente, X.S.
- Quesada, V.
- Osorio, F.G.
- Cabanillas, R.
- Cadiñanos, J.
- Fraile, J.M.
- Ordóñez, G.R.
- Puente, D.A.
- Gutiérrez-Fernández, A.
- Fanjul-Fernández, M.
- Lévy, N.
- Freije, J.M.P.
- López-Otín, C.
ISSN: 1537-6605, 0002-9297
Datum der Publikation: 2011
Ausgabe: 88
Nummer: 5
Seiten: 650-656
Art: Artikel