Blink reflex role in algorithmic genetic testing of inherited polyneuropathies

Author:

Wang Wei12ORCID,Litchy William J.1,Mandrekar Jay3,Dyck Peter J.1,Klein Christopher J.145

Affiliation:

1. Department of Neurology; Mayo Clinic; 200 First Street, SW Rochester Minnesota 55905 USA

2. Department of Neurology; China-Japan Friendship Hospital; Beijing China

3. Biomedical Statistics and Informatics; Mayo Clinic, Rochester; Minnesota USA

4. Department of Laboratory Medicine and Pathology; Mayo Clinic, Rochester; Minnesota USA

5. Department of Medical Genetics; Mayo Clinic, Rochester; Minnesota USA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference30 articles.

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2. Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy;Wang;Neurology,2016

3. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication;Wise;Am J Hum Genet,1993

4. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients;Mersiyanova;Hum Mutat,2000

5. Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing;Murphy;J Neurol Neurosurg Psychiatry,2012

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