Re‐evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome
- 1 November 2002
- journal article
- other
- Published by Wiley in American Journal of Medical Genetics
- Vol. 112 (4) , 427-428
- https://doi.org/10.1002/ajmg.10629
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Clinical study and haplotype analysis in two brothers with Partington syndromeAmerican Journal of Medical Genetics, 2002
- ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardationHuman Molecular Genetics, 2002
- Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyNature Genetics, 2002
- Linkage analysis in three families with nonspecific X-linked mental retardationAmerican Journal of Medical Genetics, 1996