Mathieu Cerino
5PUBLICATIONS
10CO-AUTHORS
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Publications (5)
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|Feb 25, 2022
A National French Consensus on Gene List for the Diagnosis of Charcot-Marie-Tooth Disease and Related Disorders Using Next-Generation Sequencing.Thibaut Benquey, Emmanuelle Pion, Mireille Cossée
|Oct 27, 2020
Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy.Mathieu Cerino, Marc Bartoli, Florence Riccardi
|Sep 16, 2020
Refining NGS diagnosis of muscular disorders.Mathieu Cerino, Emmanuelle Salort-Campana, Svetlana Gorokhova
|Jun 16, 2020
Extension of the phenotypic spectrum of GLE1-related disorders to a mild congenital form resembling congenital myopathy.Mathieu Cerino, Chloé Di Meglio, Francesca Albertini
|Apr 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathy.M Cerino, E Campana-Salort, A Salvi
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Frequent Collaborators
2 joint publications
Nathalie Bonello-Palot
2 joint publications
Mireille Cossée
2 joint publications
Marc Bartoli
1 joint publications
P Cintas
1 joint publications
C Tard
1 joint publications
T Stojkovic
1 joint publications
S Gorokhova
1 joint publications
J Mortreux
1 joint publications
S Attarian
1 joint publications
Anne-Sophie Lia
