Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patients-Reference-Cited by-同舟云学术

Mutational analysis of PMP22, GJB1 and MPZ in Greek Charcot-Marie-Tooth type 1 neuropathy patients

Published:2011-10-05 Issue:5 Volume:80 Page:497-499
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Karadima G,Floroskufi P,Koutsis G,Vassilopoulos D,Panas M

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01657.x/fullpdf

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4. Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies.;Stronach;J Peripher Nerv Syst,1999

5. Connexin mutations in X-linked Charcot-Marie-Tooth disease.;Bergoffen;Science,1993

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