Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.
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| Title: | Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. |
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| Authors: | Khan Z; Genentech, 1 DNA Way, South San Francisco, 94080, USA. khanz12@gene.com., Jung M; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Crow M; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Mohindra R; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland., Maiya V; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Kaminker JS; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Hackos DH; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Chandler GS; F. Hoffmann-La Roche, Grenzacherstrasse 124, 4070, Basel, Switzerland., McCarthy MI; Genentech, 1 DNA Way, South San Francisco, 94080, USA., Bhangale T; Genentech, 1 DNA Way, South San Francisco, 94080, USA. tusharb@gene.com. |
| Source: | Genome medicine [Genome Med] 2023 Jun 21; Vol. 15 (1), pp. 45. Date of Electronic Publication: 2023 Jun 21. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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