1. A.3 A novel recessive TNNT1 congenital core-rod myopathy in French Canadians. (June 2022) Authors: Pellerin, D; Aykanat, A; Ellezam, B; Troiano, EC; Karamchandani, J; Dicaire, M; Petitclerc, M; Robertson, R; Allard-Chamard, X; Brunet, D; Konersman, CG; Mathieu, J; Warman Chardon, J; Gupta, VA; Beggs, AH; Brais, B; Chrestian, N Journal: Canadian journal of neurological sciences Issue: Volume 49(2022)Supplement 1 Page Start: S3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A.4 A Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians. (November 2021) Authors: Pellerin, D; Aykanat, A; Ellezam, B; Troiano, EC; Karamchandani, J; Dicaire, M; Petitclerc, M; Robertson, R; Allard-Chamard, X; Brunet, D; Konersman, CG; Mathieu, J; Warman Chardon, J; Gupta, VA; Beggs, AH; Brais, B; Chrestian, N Journal: Canadian journal of neurological sciences Issue: Volume 48(2021)Supplement S3 Page Start: S14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (5th June 2019) Authors: Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (June 2019) Authors: Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. P.028 A milder congenital myopathy in the french canadians caused by a novel TNNT1 homozygous missense mutation. (5th June 2019) Authors: Pellerin, D; Aykanat, A; Ellezam, B; Karamchandani, J; Mathieu, J; Chardon, J Warman; Konersman, CG; Beggs, AH; Brais, B; Chrestian, N Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. P.028 A milder congenital myopathy in the french canadians caused by a novel TNNT1 homozygous missense mutation. (June 2019) Authors: Pellerin, D; Aykanat, A; Ellezam, B; Karamchandani, J; Mathieu, J; Chardon, J Warman; Konersman, CG; Beggs, AH; Brais, B; Chrestian, N Journal: Canadian journal of neurological sciences Issue: Volume 46(2019)Supplement 1 Page Start: S21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗