Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
Article
Gallego-Martinez, Alvaro
, Escalera-Balsera, Alba, Trpchevska, Natalia , Robles-Bolivar, Paula, Roman-Naranjo, Pablo, Frejo, Lidia, Perez-Carpena, Patricia , Bulla, Jan, Gallus, Silvano, Canlon, Barbara, Cederroth, Christopher R. and Lopez-Escamez, Jose A.
(2022)
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus.
npj Genomic Medicine 7 (1).
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| Item type | Article | ||||
| Journal or Publication Title | npj Genomic Medicine | ||||
| Publisher | Nature | ||||
| Place of Publication | BERLIN | ||||
| Volume | 7 | ||||
| Number of Issue or Book Chapter | 1 | ||||
| Date | 2022 | ||||
| Date of publication | 29 Feb 2024 13:02 | ||||
| Institutions | Medicine > Lehrstuhl für Psychiatrie und Psychotherapie | ||||
| Identification Number |
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| Keywords | JOINT CONSENSUS RECOMMENDATION; STRUCTURAL VARIANTS; MAMMALIAN HOMOLOG; MEDICAL GENETICS; AMERICAN-COLLEGE; ASSOCIATION; MECHANISMS; GUIDELINES; STANDARDS; FRAMEWORK; | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 57713 |
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