A novel splice site variant of the BBS2 gene in a patient with Bardet-Biedl syndrome

Author:

Azizi Hasan,Bonyadi MortazaORCID,Rafat Abbas

Publisher

Springer Science and Business Media LLC

Reference7 articles.

1. Akbaroghli, S. et al. Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families. Iran. J. Child Neurol. 16, 123 (2022).

2. Florea, L., Caba, L. & Gorduza, E. V. Bardet–Biedl Syndrome—Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype–Phenotype Correlations. Genes 12, 1353 (2021).

3. Suárez-González, J. et al. Novel biallelic variant in BBS9 causative of Bardet–Biedl syndrome: expanding the spectrum of disease-causing genetic alterations. BMC Med. Genom. 14, 1–5 (2021).

4. Forsyth, R. & Gunay-Aygun, M. in Bardet-Biedl Syndrome Overview. (eds Adam, M. P. et al.) GeneReviews® [Internet]. 1993–2024 (University of Washington, Seattle, 2003).

5. Dehani, M. et al. Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome. Avicenna J. Med. Biotechnol. 13, 230 (2021).

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