Escher, Pascal (2019). Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. Ophthalmic genetics, 40(6), p. 591. Taylor & Francis 10.1080/13816810.2019.1573908
![[img]](https://boris.unibe.ch/style/images/fileicons/text.png) |
Text
Escher19_proof.pdf - Accepted Version Restricted to registered users only Available under License Publisher holds Copyright. Download (140kB) |
Item Type: |
Journal Article (Further Contribution) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Ophthalmology |
UniBE Contributor: |
Escher, Pascal |
Subjects: |
600 Technology > 610 Medicine & health 500 Science > 570 Life sciences; biology |
ISSN: |
1744-5094 |
Publisher: |
Taylor & Francis |
Language: |
English |
Submitter: |
Pascal Escher |
Date Deposited: |
27 Mar 2019 17:15 |
Last Modified: |
05 Dec 2022 15:26 |
Publisher DOI: |
10.1080/13816810.2019.1573908 |
PubMed ID: |
30707043 |
BORIS DOI: |
10.7892/boris.126324 |
URI: |
https://boris.unibe.ch/id/eprint/126324 |
Actions (login required)
 |
Edit item |