Literature DB >> 1997389

No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.

K Kausch1, C R Müller, T Grimm, K Ricker, M Rietschel, S Rudnik-Schöneborn, K Zerres.   

Abstract

Two recent articles have reported the linkage of a gene for recessive spinal muscular atrophy (SMA) on the chromosome region 5q11.2-13.3. Our data show no linkage of the dominantly inherited forms of SMA to this chromosome region.

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Year:  1991        PMID： 1997389     DOI： 10.1007/bf00202419

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  6 in total

1.  Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.

Authors:  J Melki; S Abdelhak; P Sheth; M F Bachelot; P Burlet; A Marcadet; J Aicardi; A Barois; J P Carriere; M Fardeau
Journal:  Nature       Date:  1990-04-19       Impact factor: 49.962

2.  Autosomal dominant cramping disease.

Authors:  K Ricker; R T Moxley
Journal:  Arch Neurol       Date:  1990-07

3.  Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.

Authors:  L M Brzustowicz; T Lehner; L H Castilla; G K Penchaszadeh; K C Wilhelmsen; R Daniels; K E Davies; M Leppert; F Ziter; D Wood
Journal:  Nature       Date:  1990-04-05       Impact factor: 49.962

4.  Linkage analysis and family classification under heterogeneity.

Authors:  J Ott
Journal:  Ann Hum Genet       Date:  1983-10       Impact factor: 1.670

5.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

6.  Autosomal dominant spinal muscular atrophy: a clinical and genetic study.

Authors:  J Pearn
Journal:  J Neurol Sci       Date:  1978-09       Impact factor: 3.181
  6 in total
  5 in total

1.  [Motor neuron diseases].

Authors:  S Petri; T Meyer
Journal:  Nervenarzt       Date:  2011-06       Impact factor: 1.214

2.  Apparent autosomal recessive inheritance in families with proximal spinal muscular atrophy affecting individuals in two generations.

Authors:  S Rudnik-Schöneborn; K Zerres; E Hahnen; G Meng; T Voit; F Hanefeld; B Wirth
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

3.  Low segregation ratios in autosomal recessive disorders.

Authors:  S Bundey; I D Young
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

4.  Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy.

Authors:  Sabine Rudnik-Schöneborn; Elke Botzenhart; Thomas Eggermann; Jan Senderek; Benedikt G H Schoser; Rolf Schröder; Manfred Wehnert; Brunhilde Wirth; Klaus Zerres
Journal:  Neurogenetics       Date:  2006-11-29       Impact factor: 2.660

5.  Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy.

Authors:  S Rudnik-Schöneborn; B Wirth; K Zerres
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025
  5 in total

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