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Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
Holinski-Feder, E; Chahrockh-Zadeh, S; Rittinger, O; Jedele, K B; Gasteiger, M; Lenski, C; Murken, J; Golla, A.
Affiliation
  • Holinski-Feder E; Abteilung Medizinische Genetik der Kinderpoliklinik, München, Germany. elke@pedgen.med.uni-muenchen.de
Am J Med Genet ; 86(2): 102-6, 1999 Sep 10.
Article in En | MEDLINE | ID: mdl-10449641
ABSTRACT
An Austrian family with nonsyndromic X-linked mental retardation (MRX) is reported in which the obligatory carrier females are normal, and 5 affected males have mild to moderate mental retardation. Linkage analysis indicated an X pericentromeric localization, with flanking markers DXS989 and DXS1111 and a maximum multipoint LOD score of 2.09 (straight theta = 0) for the 7 cosegregating markers DXS1243, CybB, MAOB, DXS988, ALAS2, DXS991, and AR. MRX58 thus mapped within a 50-cM interval between Xp11.3 and Xq13.1 and overlapped with 23 other MRX families already described. This pericentromeric clustering of MRX families suggests allelism, with a minimum of 2 X-linked mental retardation (XLMR) genes in this region.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Intellectual Disability Limits: Female / Humans / Male Language: En Journal: Am J Med Genet Year: 1999 Document type: Article Affiliation country: Germany
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Intellectual Disability Limits: Female / Humans / Male Language: En Journal: Am J Med Genet Year: 1999 Document type: Article Affiliation country: Germany