Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia.
Autor: | Zanni G, Saillour Y, Nagara M, Billuart P, Castelnau L, Moraine C, Faivre L, Bertini E, Durr A, Guichet A, Rodriguez D, des Portes V, Beldjord C, Chelly J, Zanni, G, Saillour, Y, Nagara, M, Billuart, P, Castelnau, L, Moraine, C |
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Zdroj: | Neurology; 2005 Nov 8, Vol. 65 Issue 9, p1364-1369, 6p |
Databáze: | Complementary Index |
Externí odkaz: |