A knockin mouse model of the Bardet–Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

Overview of attention for article published in Proceedings of the National Academy of Sciences of the United States of America, December 2007

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GENE THERAPY FOR BARDET-BIEDL SYNDROME

Application WO-2021209772-A3

World Intellectual Property Organisation (WIPO)

Methods and compositions for universal size-specific PCR

Grant US-9404150-B2

United States of America

Detection and quantification of biomolecules using mass spectrometry

Grant US-9051608-B2

United States of America

COMPOSITIONS AND METHODS FOR THE TREATMENT OF RETINAL DEGENERATION

Application WO-2013124484-A1

World Intellectual Property Organisation (WIPO)

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