Amr Al-Saif

Summary

Affiliation: King Faisal Specialist Hospital and Research Centre
Country: Saudi Arabia

Publications

  1. ncbi Loss of ERLIN2 function leads to juvenile primary lateral sclerosis
    Amr Al-Saif
    Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Ann Neurol 72:510-6. 2012
  2. ncbi A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
    Amr Al-Saif
    Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Ann Neurol 70:913-9. 2011

Detail Information

Publications2

  1. ncbi Loss of ERLIN2 function leads to juvenile primary lateral sclerosis
    Amr Al-Saif
    Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Ann Neurol 72:510-6. 2012
    ..In this study, we identify mutation of the ERLIN2 gene in juvenile PLS patients and describe an in vitro model for loss of ERLIN2 function...
  2. ncbi A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
    Amr Al-Saif
    Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Ann Neurol 70:913-9. 2011
    ..Here we describe a consanguineous family segregating juvenile ALS in an autosomal recessive pattern and describe the genetic variant responsible for the disorder...