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Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.

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Title: Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.
Authors: Tu, Wei-Ting1 (AUTHOR), Hou, Ping-Chen1 (AUTHOR), Chen, Peng-Chieh2 (AUTHOR), Chen, Wan-Rung1 (AUTHOR), Huang, Hsin-Yu1 (AUTHOR), Wang, Jing-Yu3 (AUTHOR), Huang, Yi-Ting3 (AUTHOR), Wu, Yi-Huei4 (AUTHOR), Su, Chun-Lin5 (AUTHOR), Tang, Yen-An6,7 (AUTHOR), Iwata, Hiroaki8 (AUTHOR), Natsuga, Ken8 (AUTHOR), Chao, Sheau-Chiou1 (AUTHOR), Sun, H. Sunny6,7 (AUTHOR), Tang, Ming-Jer5 (AUTHOR), Lee, Julia Yu-Yun1 (AUTHOR), McGrath, John A.9 (AUTHOR), Hsu, Chao-Kai1,2,5 (AUTHOR) kylehsu@mail.ncku.edu.tw
Source: Orphanet Journal of Rare Diseases. 12/28/2022, Vol. 17 Issue 1, p1-10. 10p.
Database: Academic Search Ultimate
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  Data: Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 12/28/2022, Vol. 17 Issue 1, p1-10. 10p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=161029662
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        Value: 10.1186/s13023-022-02605-1
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              Text: 12/28/2022
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              Y: 2022
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