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Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia
Bergmann, C.; Zerres, K.; Senderek, J. et al.
2003 • In Brain: a Journal of Neurology, 126 (7), p. 1537-1544

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

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