Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome

1. Puente, X.S.
2. Quesada, V.
3. Osorio, F.G.
4. Cabanillas, R.
5. Cadiñanos, J.
6. Fraile, J.M.
7. Ordóñez, G.R.
8. Puente, D.A.
9. Gutiérrez-Fernández, A.
10. Fanjul-Fernández, M.
11. Lévy, N.
12. Freije, J.M.P.
13. López-Otín, C.

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DOI: 10.1016/J.AJHG.2011.04.010 GOOGLE SCHOLAR lock_openOpen access editor

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