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Robin Paluch

1PUBLICATIONS

85CO-AUTHORS

Neurology and neuromuscular diseases

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Publications (1)

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|Mar 30, 2026

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

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Frequent Collaborators

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Elsa Leitão

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Amandine Santini

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Benjamin Cogne

1 joint publications

Miriam Essid

1 joint publications

Maria Athanasiadou

1 joint publications

Christy W LaFlamme

1 joint publications

Pierre Marijon

1 joint publications

Nicolas Chatron

1 joint publications

Thomas Besnard

1 joint publications

Jean-Madeleine de Sainte Agathe

Frequent Collaborators

1 joint publications

Elsa Leitão

1 joint publications

Amandine Santini

1 joint publications

Benjamin Cogne

1 joint publications

Miriam Essid

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