Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics

This publication has 24 references indexed in Scilit:

• SMN oligomerization defect correlates with spinal muscular atrophy severity
  Nature Genetics, 1998
• Matrin CYP, an SR-rich Cyclophilin That Associates with the Nuclear Matrix and Splicing Factors
  Journal of Biological Chemistry, 1998
• The Spinal Muscular Atrophy Disease Gene Product, SMN, and Its Associated Protein SIP1 Are in a Complex with Spliceosomal snRNP Proteins
  Cell, 1997
• The survival motor neuron protein in spinal muscular atrophy
  Human Molecular Genetics, 1997
• Correlation between severity and SMN protein level in spinal muscular atrophy
  Nature Genetics, 1997
• The Mouse Region Syntenic for Human Spinal Muscular Atrophy Lies within theLgn1Critical Interval and Contains Multiple Copies ofNaipExon 5
  Genomics, 1996
• Identification and characterization of a spinal muscular atrophy-determining gene
  Cell, 1995
• International SMA Consortium Meeting (26–28 June 1992, Bonn, Germany)
  Neuromuscular Disorders, 1992
• Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14
  The Lancet, 1990
• Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
  Nature, 1990