Severe CMD with Novel Mutation in Lamin A/C Gene

Open Access

|Nov 2010

Prigogine C Richard P Van den Bergh P Groswasser J Deconinck N Novel LMNA mutation presenting as severe congenital muscular dystrophy Pediatr Neurol 2010 Oct 43 4 283 6 10.1016/j.pediatrneurol.2010.05.016 20837309
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Quijano-Roy S Mbieleu B Bönnemann CG Jeannet PY Colomer J Clarke NF De novo LMNA mutations cause a new form of congenital muscular dystrophy Ann Neurol 2008 Aug 64 2 177 86 10.1002/ana.21417 18551513
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Language: English

Page range: 88 - 88

Published on: Nov 1, 2010

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

© 2010 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.