Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)-Reference-Cited by-同舟云学术

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

Published:2018-01-01 Issue:1 Volume:12 Page:17-33
ISSN:1933-6950
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language:en
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Author:

Waldner D. M.¹,Giraldo Sierra N. C.²,Bonfield S.¹,Nguyen L.²,Dimopoulos I. S.³,Sauvé Y.³⁴,Stell W. K.⁵^ORCID,Bech-Hansen N. T.⁶

Affiliation:

1. Department of Neuroscience, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

2. Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

3. Department of Ophthalmology and Visual Sciences, University of Alberta, Edmonton, Alberta, Canada

4. Department of Physiology, University of Alberta, Edmonton, Alberta, Canada

5. Department of Cell Biology and Anatomy and Department of Surgery, Hotchkiss Brain Institute, and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

6. Department of Medical Genetics, and Department of Surgery, Alberta Children's Hospital Research Institute, and Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

Funder

Foundation Fighting Blindness

Alberta Ride for Sight

Lions Sight Centre Fund

CIHR - Operating Grant - N.T. Bech-Hansen - ntbech@ucalgary.ca

NSERC - Discovery Grant - W.K. Stell - wstell@ucalgary.ca

Publisher

Informa UK Limited

Subject

Biochemistry,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336950.2017.1401688