Sturm, V; Leiba, H; Menke, M N; Valente, E M; Poretti, A; Landau, K; Boltshauser, E (2010). Ophthalmological findings in Joubert syndrome. Eye, 24(2), pp. 222-225. London: Nature Publishing Group 10.1038/eye.2009.116
Full text not available from this repository. (Request a copy)Joubert syndrome (JS) is an autosomal-recessive inherited complex malformation of the midbrain-hindbrain. It has been associated with ocular and oculomotor abnormalities. The aim of our study was to extend the ophthalmic knowledge in JS and to add new findings.
Item Type: |
Journal Article (Original Article) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Ophthalmology |
UniBE Contributor: |
Menke, Marcel |
ISSN: |
0950-222X |
Publisher: |
Nature Publishing Group |
Language: |
English |
Submitter: |
Factscience Import |
Date Deposited: |
04 Oct 2013 14:08 |
Last Modified: |
05 Dec 2022 14:00 |
Publisher DOI: |
10.1038/eye.2009.116 |
PubMed ID: |
19461662 |
Web of Science ID: |
000274397900003 |
URI: |
https://boris.unibe.ch/id/eprint/306 (FactScience: 197486) |
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