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R. de Cid
R. de Cid
French Institute of Health and Medical Research
Genetics
Biology
Muscular dystrophy
Exome sequencing
Cardiac abnormality
2
Papers
1
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0
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Exome sequencing identifies novel truncating TTN mutations with Emery–Dreifuss like muscular dystrophy and secondary calpain3 deficiency without cardiac abnormality
2015
Neuromuscular Disorders
R. de Cid
R. Ben Yaou
C. Roudaut
Sylvain Baulande
F. Leturcq
G. Bonne
Bjarne Udd
Norma B. Romero
K. Charton
E. Malfatti
I. Nelson
B. Eymard
I Richard
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G.P.281
2014
Neuromuscular Disorders
Juliette Nectoux
R. de Cid
Sylvain Baulande
F. Leturcq
Jon Andoni Urtizberea
I. Pénisson-Besnier
A. Nadaj Pakleza
C. Roudaut
Audrey Criqui
Lucie Orhant
D. Peyroulan
R. Ben Yaou
I. Nelson
Marie Christine Arne Bes
Patrick Nitschke
Mireille Claustres
G. Bonne
Nicolas Lévy
Jamel Chelly
I Richard
Mireille Cossée
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