Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder-Reference-Cited by-同舟云学术

Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder

Published:2022-01 Issue: Volume:524 Page:51-58
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Rochdi Khaoula,Cerino Mathieu,Da Silva Nathalie,Delague Valerie,Bouzidi Aymane,Nahili Halima,Zouiri Ghizlane,Kriouile Yamna,Gorokhova Svetlana,Bartoli Marc,Saïle Rachid,Barakat Abdelhamid,Krahn Martin

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference69 articles.

1. Morrison. Neuromuscular diseases. (2016).

2. The Epidemiology of Neuromuscular Diseases;Bhatt;Neurol. Clin.,2016

3. Neuromuscular disease and respiratory failure;Hutchinson;Pract. Neurol.,2008

4. Genetics of neuromuscular disorders;Laing;Crit. Rev. Clin. Lab. Sci.,2012

5. First characterization of congenital myasthenic syndrome type 5 in North Africa;Khaoula;Mol. Biol. Rep.,2021

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