M Ghannad

Summary

Affiliation: University of British Columbia
Country: Canada

Publications

  1. doi request reprint The essential role of NDE1 in extreme microcephaly
    M Ghannad
    Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada E mail
    Clin Genet 80:241-2. 2011
  2. doi request reprint DNMT1 links aberrant DNA methylation to hereditary sensory neuropathy
    M Ghannad
    Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada E mail
    Clin Genet 80:240-1. 2011

Detail Information

Publications2

  1. doi request reprint The essential role of NDE1 in extreme microcephaly
    M Ghannad
    Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada E mail
    Clin Genet 80:241-2. 2011
    ..2011) The American Journal of Human Genetics 88: 523-535 Human mutations in NDE1 cause extreme microcephaly with lissencephaly Alkuraya et al. (2011) The American Journal of Human Genetics 88: 536-547...
  2. doi request reprint DNMT1 links aberrant DNA methylation to hereditary sensory neuropathy
    M Ghannad
    Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada E mail
    Clin Genet 80:240-1. 2011
    ..Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss Klein et al. (2011) Nature Genetics. Advanced online publication...