P.133 Expanding the phenotype of TRNT1 mutations to include Leigh syndrome
Gorodetsky, C, Morel, CF, Tein, I
Published in Canadian journal of neurological sciences (01.06.2018)
Published in Canadian journal of neurological sciences (01.06.2018)
Get full text
Journal Article
Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizures
Vincent, AK, Noor, A, Janson, A, Minassian, BA, Ayub, M, Vincent, JB, Morel, CF
Published in Clinical genetics (01.12.2012)
Published in Clinical genetics (01.12.2012)
Get full text
Journal Article