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Correction: Mutations in thePLEKHG5gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

✍ Scribed by Hyeon Jin Kim,Young Bin Hong,Jin-Mo Park,Yu-Ri Choi…


Book ID
126377677
Publisher
BioMed Central
Year
2013
Tongue
English
Weight
104 KB
Volume
8
Category
Article
ISSN
1750-1172

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Charcot–marie–tooth disease with interme
✍ Isabel Banchs; Carlos Casasnovas; Jordi Montero; Victor Volpini; Juan Antonio Ma 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 511 KB

## Abstract Charcot–Marie–Tooth (CMT) disease is a heterogeneous group of inherited sensory and motor neuropathies. Mutations in the gene that encodes for myelin protein zero (__MPZ__) can produce different phenotypes: CMT1 (with low conduction velocities), CMT2 (less frequent and with unaffected c