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Louise R Simard

1PUBLICATIONS

3CO-AUTHORS

Neurology and neuromuscular diseases

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Publications (1)

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|Dec 18, 2018

A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families.

Jessica N Hartley, Louise R Simard, Valentina Ly

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Frequent Collaborators

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Jessica N Hartley

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Marc R Del Bigio

1 joint publications

Patrick Frosk

Frequent Collaborators

1 joint publications

Jessica N Hartley

1 joint publications

Marc R Del Bigio

1 joint publications

Patrick Frosk

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