Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophy

17 Feb 2016

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy and Myosin Studies
Share to Muscle Physiology and Disorders
Share to Neurogenetic and Muscular Disorders Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26886200
DOI: 10.1007/s00415-016-8036-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophyPMID 26886200Read ↗

Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophySemantic proximity Read ↗

Molecular genetic testing and diagnosis strategies for dystrophinopathies in the era of next generation sequencingSemantic proximity Read ↗

Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies.Semantic proximity Read ↗

Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy.Semantic proximity Read ↗

Clinical applications of next‐generation sequencing‐based gene panel in patients with muscular dystrophy: Korean experienceSemantic proximity Read ↗

Best practice guidelines on genetic diagnostics of Facioscapulohumeral muscular dystrophy: Workshop 9th June 2010, LUMC, Leiden, The NetherlandsSemantic proximity Read ↗

Large-Scale Population Analysis Challenges the Current Criteria for the Molecular Diagnosis of Fascioscapulohumeral Muscular DystrophySemantic proximity Read ↗

The rapid evolution of molecular genetic diagnostics in neuromuscular diseasesSemantic proximity Read ↗

Guidelines for genetic testing of muscle and neuromuscular junction disorders.Semantic proximity Read ↗

Approaches to genetic diagnosis in neuromuscular conditions in the era of next generation sequencing.Semantic proximity Read ↗

Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic.Semantic proximity Read ↗

A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.