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Showing results (41-50 of 46) with videos related to

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Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Neurologia|April 21, 2019
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's diseaseG Gutiérrez Gutiérrez, J Díaz-Manera, M Almendrote, et al.
Neurologia|March 2, 2024
Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth diseaseR Sivera Mascaró, T García Sobrino, A Horga Hernández, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
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Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.
Neuromuscular Disorders : NMD|October 22, 2017
Molecular characterization of congenital myasthenic syndromes in SpainD Natera-de Benito, A Töpf, J J Vilchez, et al.
Neurologia|April 21, 2019
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's diseaseG Gutiérrez Gutiérrez, J Díaz-Manera, M Almendrote, et al.
Neurologia|March 2, 2024
Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth diseaseR Sivera Mascaró, T García Sobrino, A Horga Hernández, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
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