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Publications by Jean-Pierre Lin

Brown-Vialetto-Van Laere Syndrome, a Ponto-Bulbar Palsy With Deafness, Is Caused by Mutations in C20orf54

American Journal of Human Genetics

English

Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias

Frontiers in Neurology

English

Progression to Musculoskeletal Deformity in Childhood Dystonia

European Journal of Paediatric Neurology

English

Acetylcholine Receptor Δ Subunit Mutations Underlie a Fast-Channel Myasthenic Syndrome and Arthrogryposis Multiplex Congenita

Journal of Clinical Investigation

English

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Sequencing Studies in Human Genetics: Design and Interpretation

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Putting Gene Essentiality Into Context

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