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Bruno Eymard

2PUBLICATIONS

20CO-AUTHORS

Cell physiologyGene and molecular therapy

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Publications (2)

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|Nov 26, 2025

C-terminal extension of HSPB6 in a family with myopathy and cataract.

Jaakko Sarparanta, Per Harald Jonson, Anna Vihola

|Mar 04, 2021

New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromes.

Stéphanie Bauché, Alain Sureau, Damien Sternberg

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Frequent Collaborators

1 joint publications

Stéphanie Bauché

1 joint publications

Alain Sureau

1 joint publications

Damien Sternberg

1 joint publications

John Rendu

1 joint publications

Denis Furling

1 joint publications

Antoinette Bernabe Gelot

1 joint publications

Sandra Whalen

1 joint publications

Emmanuel Fournier

1 joint publications

Ganaelle Remerand

1 joint publications

Bertrand Fontaine

Frequent Collaborators

1 joint publications

Stéphanie Bauché

1 joint publications

Alain Sureau

1 joint publications

Damien Sternberg

1 joint publications

John Rendu

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