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

By Ramser Juliane  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1019-1027

Oxford University Press

Access to resources Recommend Favorite

Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation

By Chelly Jamel  

Human Molecular Genetics, Vol. 8, Iss. 10, 1999-10 ,pp. : 1833-1838

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

A Model of Corrective Gene Transfer in X-Linked Ichthyosis

By Freiberg Rachel A.  

Human Molecular Genetics, Vol. 6, Iss. 6, 1997-01 ,pp. : 927-933

Oxford University Press

Access to resources Recommend Favorite

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

By Ropers H-H.  

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

Oxford University Press

Access to resources Recommend Favorite