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He, Longxia, Pang, Xiuhong, Chen, Penghui, Wang, Xiaowen, Yang, Tao, Wu, Hao (2017) Carrier re-sequencing reveals rare but benign variants in recessive deafness genes. Scientific Reports, 7. doi:10.1038/s41598-017-10099-2

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Reference TypeJournal (article/letter/editorial)
TitleCarrier re-sequencing reveals rare but benign variants in recessive deafness genes
JournalScientific Reports
AuthorsHe, LongxiaAuthor
Pang, XiuhongAuthor
Chen, PenghuiAuthor
Wang, XiaowenAuthor
Yang, TaoAuthor
Wu, HaoAuthor
Year2017 (December)Volume7
PublisherSpringer Science and Business Media LLC
DOIdoi:10.1038/s41598-017-10099-2Search in ResearchGate
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Mindat Ref. ID4683442Long-form Identifiermindat:1:5:4683442:7
GUID0
Full ReferenceHe, Longxia, Pang, Xiuhong, Chen, Penghui, Wang, Xiaowen, Yang, Tao, Wu, Hao (2017) Carrier re-sequencing reveals rare but benign variants in recessive deafness genes. Scientific Reports, 7. doi:10.1038/s41598-017-10099-2
Plain TextHe, Longxia, Pang, Xiuhong, Chen, Penghui, Wang, Xiaowen, Yang, Tao, Wu, Hao (2017) Carrier re-sequencing reveals rare but benign variants in recessive deafness genes. Scientific Reports, 7. doi:10.1038/s41598-017-10099-2
In(2017) Scientific Reports Vol. 7. Springer Science and Business Media LLC

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