De novoLMNAmutations cause a new form of congenital muscular dystrophy-Reference-Cited by-同舟云学术

De novoLMNAmutations cause a new form of congenital muscular dystrophy

Published:2008-08 Issue:2 Volume:64 Page:177-186
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Quijano-Roy Susana,Mbieleu Blaise,Bönnemann Carsten G.,Jeannet Pierre-Yves,Colomer Jaume,Clarke Nigel F.,Cuisset Jean-Marie,Roper Helen,De Meirleir Linda,D'Amico Adele,Ben Yaou Rabah,Nascimento Andrés,Barois Annie,Demay Laurence,Bertini Enrico,Ferreiro Ana,Sewry Caroline A.,Romero Norma B.,Ryan Monique,Muntoni Francesco,Guicheney Pascale,Richard Pascale,Bonne Gisèle,Estournet Brigitte

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference35 articles.

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4. Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant;Mercuri;Arch Neurol,2004

5. Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene;Mercuri;Muscle Nerve,2005

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