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Author/Creator Cyr, Denis

1. HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec. Issue 12 (26th October 2019)

Authors:
Waters, Paula J.; Lace, Baiba; Buhas, Daniela; Gravel, Serge; Cyr, Denis; Boucher, Renée‐Myriam; Bernard, Geneviève; Lévesque, Sébastien; Maranda, Bruno
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 12(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Hypersuccinylacetonaemia and normal liver function in maleylacetoacetate isomerase deficiency. Issue 4 (22nd November 2016)

Authors:
Yang, Hao; Al-Hertani, Walla; Cyr, Denis; Laframboise, Rachel; Parizeault, Guy; Wang, Shu Pei; Rossignol, Francis; Berthier, Marie-Thérèse; Giguère, Yves; Waters, Paula J; Mitchell, Grant A
Other Names:
author non-byline.; Alvarez Fernando author non-byline.; Brunel-Guitton Catherine author non-byline.; Buhas Daniela author non-byline.; Dubois Josée author non-byline.; Gosselin Martyne author non-byline.; Halac Ugur author non-byline.; Maranda Bruno author non-byline.; Mitchell John author non-...
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 4(2017)
Page Start:
241
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗