Your browser doesn't support javascript.
loading
Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation.
Pandolfo, Massimo; Rai, Myriam; Remiche, Gauthier; Desmyter, Laurence; Vandernoot, Isabelle.
Affiliation
  • Pandolfo M; Neurology Service (M.P., G.R.), Hôpital Erasme; Laboratory of Experimental Neurology (M.P., M.R.); and Medical Genetics Service (L.D., I.V.), Hôpital Erasme, Université Libre de Bruxelles, Belgium.
  • Rai M; Neurology Service (M.P., G.R.), Hôpital Erasme; Laboratory of Experimental Neurology (M.P., M.R.); and Medical Genetics Service (L.D., I.V.), Hôpital Erasme, Université Libre de Bruxelles, Belgium.
  • Remiche G; Neurology Service (M.P., G.R.), Hôpital Erasme; Laboratory of Experimental Neurology (M.P., M.R.); and Medical Genetics Service (L.D., I.V.), Hôpital Erasme, Université Libre de Bruxelles, Belgium.
  • Desmyter L; Neurology Service (M.P., G.R.), Hôpital Erasme; Laboratory of Experimental Neurology (M.P., M.R.); and Medical Genetics Service (L.D., I.V.), Hôpital Erasme, Université Libre de Bruxelles, Belgium.
  • Vandernoot I; Neurology Service (M.P., G.R.), Hôpital Erasme; Laboratory of Experimental Neurology (M.P., M.R.); and Medical Genetics Service (L.D., I.V.), Hôpital Erasme, Université Libre de Bruxelles, Belgium.
Neurol Genet ; 6(3): e420, 2020 Jun.
Article in En | MEDLINE | ID: mdl-32337346
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Neurol Genet Year: 2020 Document type: Article Affiliation country: Bélgica
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Neurol Genet Year: 2020 Document type: Article Affiliation country: Bélgica