Oligophrenin 1 ( OPHN1 ) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

Author： Bergmann C.  

Publisher： Oxford University Press

ISSN： 1460-2156

Source： Brain, Vol.126, Iss.7, 2003-07, pp. : 1537-1544

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