Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.

Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.

With the advent of whole exome sequencing, cases where no pathogenic coding mutations can be found are increasingly being observed in many diseases. In two large, distantly-related families that mapped to the Charcot-Marie-Tooth neuropathy CMTX3 locus at chromosome Xq26.3-q27.3, all coding mutations...

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Бібліографічні деталі
Автори: Megan H Brewer, Rabia Chaudhry, Jessica Qi, Aditi Kidambi, Alexander P Drew, Manoj P Menezes, Monique M Ryan, Michelle A Farrar, David Mowat, Gopinath M Subramanian, Helen K Young, Stephan Zuchner, Stephen W Reddel, Garth A Nicholson, Marina L Kennerson
Формат: Стаття
Мова:English
Опубліковано: Public Library of Science (PLoS) 2016-07-01
Серія:PLoS Genetics
Онлайн доступ:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006177&type=printable

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https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006177&type=printable

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