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A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation

Archive ouverte | Zemni, Ramzi | CCSD

International audience

Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardation

Archive ouverte | Des Portes, Vincent | CCSD

International audience. X-linked mental retardation (XLMR) is a genetically and clinically heterogeneous common disorder. A cumulative frequency of about 1/600 male births was estimated by different authors, includi...

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

Archive ouverte | Billuart, Pierre | CCSD

Primary or nonspecific X-linked mental retardation (MRX) is a heterogeneous condition in which affected patients do not have any distinctive clinical or biochemical features in common apart from cognitive impairment. Although it i...

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