Double-trouble in pediatric neurology: Myotonia congenita combined with charcot-marie-tooth disease type 1a-Reference-Cited by-同舟云学术

Double-trouble in pediatric neurology: Myotonia congenita combined with charcot-marie-tooth disease type 1a

Author:

Ardissone Anna¹,Brugnoni Raffaella²,Gandioli Claudia¹,Milani Micaela³,Ciano Claudia⁴,Uziel Graziella¹,Moroni Isabella¹

Affiliation:

1. Child Neurology Unit; Foundation IRCCS “Carlo Besta” Neurological Institute; Milan Italy

2. Neuromuscular Diseases and Neuroimmunology Unit; Foundation IRCCS “Carlo Besta” Neurological Institute; Milan Italy

3. Genetics of Neurodegenerative and Metabolic Diseases Unit; Foundation IRCCS “Carlo Besta” Neurological Institute; Milan Italy

4. Neurophysiopathology and Epilepsy Unit; Foundation IRCCS “Carlo Besta” Neurological Institute; Milan Italy

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference13 articles.

1. Myotonia congenita;Lossin;Adv Genet,2008

5. Diagnostics and therapy of muscle channelopathies-guidelines of the Ulm Muscle Centre;Lehmann-Horn;Acta Myol,2008

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