Baseline characteristics of patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

Annoussamy, M.; Grangé, A.; Lilien, C.; Chê, V.; Duchêne, D.; Gidaro, T.; Behin, A.; Baets, J.; D'Amico, A.; DARON, Aurore; Bitoun, M.; Paradis, K.; Thielemans, L.; Van Rooijen, S.; Servais, Laurent

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Baseline characteristics of patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

Annoussamy, M.; Grangé, A.; Lilien, C. et al.

2018 • WMS Congress 2018

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https://hdl.handle.net/2268/232315

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Disciplines :

Neurology
Pediatrics

Author, co-author :

Annoussamy, M.

Grangé, A.

Lilien, C.

Chê, V.

Duchêne, D.

Gidaro, T.

Behin, A.

Baets, J.

D'Amico, A.

DARON, Aurore ; Centre Hospitalier Universitaire de Liège - CHU > Département de Pédiatrie > Service de pédiatrie

More authors (5 more)

Language :

English

Title :

Baseline characteristics of patients with centronuclear myopathy due to mutations in DNM2 gene enrolled in a European prospective natural history study

Publication date :

October 2018

Event name :

WMS Congress 2018

Event place :

Mendoza, Argentina

Event date :

Du 2 au 6 octobre 2018

Audience :

International

Available on ORBi :

since 29 January 2019

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