Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy.

Escher, Pascal (2019). Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. (In Press). Ophthalmic genetics, p. 1. Taylor & Francis 10.1080/13816810.2019.1573908

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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:

28 Mar 2019 01:32

Publisher DOI:

10.1080/13816810.2019.1573908

PubMed ID:

30707043

BORIS DOI:

10.7892/boris.126324

URI:

https://boris.unibe.ch/id/eprint/126324

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