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Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population

✍ Scribed by Myriam Srour; Jeremy Schwartzentruber; Fadi F. Hamdan; Luis H. Ospina; Lysanne Patry; Damian Labuda; Christine Massicotte; Sylvia Dobrzeniecka; José-Mario Capo-Chichi; Simon Papillon-Cavanagh; Mark E. Samuels; Kym M. Boycott; Michael I. Shevell; Rachel Laframboise; Valérie Désilets; Bruno Maranda; Guy A. Rouleau; Jacek Majewski; Jacques L. Michaud


Book ID
113423193
Publisher
American Society of Human Genetics
Year
2012
Tongue
English
Weight
531 KB
Volume
90
Category
Article
ISSN
0002-9297

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