Multi-Minicore and Central Core Disease
DOI:
https://doi.org/10.15844/pedneurbriefs-16-6-9Keywords:
Ryanodine Receptor Type, Axial Weakness, Homozygous Missense MutationAbstract
A genome-wide screening was conducted in a consanguinous Algerian family with 3 children with multicore disease at the Groupe Hospitalier Pitie-Salpetriere, Paris, France, and other centers.Published
2002-06-01
Issue
Section
Muscle Disorders
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Copyright (c) 2002 The Author(s)
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