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Paper Details

The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy.
Genet Med
16
2016
Alu, CMT, CMT genes, CMT1, CMT1A, CMT1A duplication, CNVs, Charcot-Marie-Tooth (CMT) disease, MFN2 SNVs, PMP22, PMP22 locus, SNVs, disease-associated locus, distal symmetric polyneuropathy, genetic disorders of the peripheral nervous system, neuropathy, neuropathy genes, patients, single-nucleotide variants
Author NameAffiliation
Christine R BeckBaylor College of Medicine
Zeynep Coban AkdemirBaylor College of Medicine
Shalini N JhangianiBaylor College of Medicine
Marjorie WithersBaylor College of Medicine
Wojciech WiszniewskiBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
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