Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z withMORC2mutations
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/139/7/e40/17348859/aww082.pdf
Reference12 articles.
1. MORC2mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs
2. A cohort study ofMFN2mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients
3. The CpG dinucleotide and human genetic disease
4. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis
5. X-linked Charcot-Marie-Tooth disease type 6 (CMTX6) patients with a p.R158H mutation in the pyruvate dehydrogenase kinase isoenzyme 3 gene
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