Inherited disorders of the neuromuscular junction: an update.

Inherited disorders of the neuromuscular junction: an update.

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http://www.wikidata.org/entity/Q38259083
Drosophila tools and assays for the study of human diseasesCongenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain.Myasthenia gravis: a clinical-immunological update.Clinical features of the myasthenic syndrome arising from mutations in GMPPB.Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.Low-Density Lipoprotein Receptor-Related Proteins in Skeletal Development and Disease.Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders.Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation.Beta-2 Adrenergic Receptor Agonists Enhance AChR Clustering in C2C12 Myotubes: Implications for Therapy of Myasthenic Disorders.Animal Models of the Neuromuscular Junction, Vitally Informative for Understanding Function and the Molecular Mechanisms of Congenital Myasthenic Syndromes.
P2860

Inherited disorders of the neuromuscular junction: an update.

Item
http://www.wikidata.org/entity/Q38259083
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
Inherited disorders of the neuromuscular junction: an update.
@en
type
label
Inherited disorders of the neuromuscular junction: an update.
@en
prefLabel
Inherited disorders of the neuromuscular junction: an update.
@en
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P6179
P698
P356
P1433
P1476
Inherited disorders of the neuromuscular junction: an update.
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P6179
P698