Mutational analysis ofGJB1,MPZ,PMP22,EGR2, andLITAF/SIMPLEin Serbian Charcot-Marie-Tooth patients-Reference-Cited by-同舟云学术

Mutational analysis ofGJB1,MPZ,PMP22,EGR2, andLITAF/SIMPLEin Serbian Charcot-Marie-Tooth patients

Published:2009-06 Issue:2 Volume:14 Page:125-136
ISSN:1085-9489
Container-title:Journal of the Peripheral Nervous System
language:en
Short-container-title:

Author:

Keckarevic-Markovic Milica,Milic-Rasic Vedrana,Mladenovic Jelena,Dackovic Jelena,Kecmanovic Miljana,Keckarevic Dusan,Savic-Pavicevic Dusanka,Romac Stanka

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1529-8027.2009.00222.x/fullpdf

Reference49 articles.

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3. Connexin32 and X-linked Charcot-Marie-Tooth disease;Bone;Neurobiol Dis,1997

4. Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies;Bort;Hum Genet,1997

5. DNA deletion associated with hereditary neuropathy with liability to pressure palsies;Chance;Cell,1993

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3. Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype;Journal of Neurology;2019-07-05

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5. Genotype–phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in theMPZgene;Brain;2015-08-25