A cohort study ofMFN2mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients
about
Identification of Genetic Causes of Inherited Peripheral Neuropathies by Targeted Gene Panel SequencingMitochondrial fusion, fission, and mitochondrial toxicity.Deficiencies in mitochondrial dynamics sensitize Caenorhabditis elegans to arsenite and other mitochondrial toxicants by reducing mitochondrial adaptability.Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients.Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case study.Regulation of mitophagy by the ubiquitin pathway in neurodegenerative diseases.Charcot-Marie-Tooth disease type 2A with an autosomal-recessive inheritance: the first report of an adult-onset disease.Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations.
P2860
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P2860
A cohort study ofMFN2mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients
description
im Juni 2014 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 18 June 2014
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wetenschappelijk artikel
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наукова стаття, опублікована в червні 2014
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name
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@en
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@nl
type
label
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@en
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@nl
prefLabel
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@en
A cohort study ofMFN2mutations ...... arie-Tooth disease 2A patients
@nl
P2093
P2860
P356
P1433
P1476
A cohort study of MFN2 mutatio ...... arie-Tooth disease 2A patients
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P2093
P2860
P304
P356
10.1111/CGE.12432
P577
2014-06-18T00:00:00Z