MECP2 is highly mutated in X-linked mental retardation

By Souville I.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 941-946

Oxford University Press

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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

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Oxford University Press

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Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor

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Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1311-1315

Oxford University Press

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Cloning and Characterization of DXS6673E , a Candidate Gene for X-linked Mental Retardation in Xq13.1

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

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