An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth-Reference-Cited by-同舟云学术

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An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth

Published:2013-01 Issue:1 Volume:17 Page:85-87
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Keckarevic Markovic Milica P.¹,Dackovic Jelena²,Mladenovic Jelena³,Milic-Rasic Vedrana⁴³,Kecmanovic Miljana¹,Keckarevic Dusan¹,Romac Stanka¹

Affiliation:

1. Faculty of Biology, University of Belgrade, Belgrade, Serbia.

2. Clinic of Neurology, Clinical Center of Serbia, Belgrade, Serbia.

3. Clinic of Neurology and Psychiatry for Children and Youth, Clinical Center of Serbia, Belgrade, Serbia.

4. Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2012.0238

Reference10 articles.

1. N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom

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

3. Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

4. Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families

5. Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients;Neuromuscular Disorders;2016-10

2. Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats;Clinical Chemistry and Laboratory Medicine (CCLM);2016-01-01

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