Carolin Mattausch
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85CO-AUTHORS
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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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Elsa Leitão
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Amandine Santini
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Benjamin Cogne
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Miriam Essid
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Maria Athanasiadou
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Christy W LaFlamme
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Pierre Marijon
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Nicolas Chatron
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Thomas Besnard
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Robin Paluch
