X-linked mental deficiency
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Publisher
Elsevier
Reference49 articles.
1. The mGluR theory of fragile X mental retardation;Bear;Trends Neurosci,2004
2. Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia;Bergmann;Brain,2003
3. Five years of molecular diagnosis of Fragile X syndrome (1997–2001): a collaborative study reporting 95% of the activity in France;Biancalana;Am J Med Genet,2004
4. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation;Bienvenu;Hum Mol Genet,2002
5. Oligophrenin 1, a novel gene encoding a rho-GAP protein involved in X-linked non-specific mental retardation;Billuart;Nature,1998
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