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A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family

Nikopoulos, K. and Butt, G. U. and Farinelli, P. and Mudassar, M. and Domènech-Estévez, E. and Samara, C. and Kausar, M. and Masroor, I. and Chrast, R. and Rivolta, C. and Siddiqi, S.. (2016) A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family. Clinical Genetics, 89 (4). pp. 510-511.

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Official URL: https://edoc.unibas.ch/82128/

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Faculties and Departments:03 Faculty of Medicine
09 Associated Institutions > Institute of Molecular and Clinical Ophthalmology Basel (IOB)
UniBasel Contributors:Rivolta, Carlo
Item Type:Article, refereed
Article Subtype:Further Journal Contribution
Publisher:John Wiley & Sons, Inc
ISSN:1399-0004
Note:Publication type according to Uni Basel Research Database: Journal item
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Last Modified:12 Apr 2021 08:53
Deposited On:12 Apr 2021 08:53

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