1-2 of 2
Keywords: Bardet-Biedl syndrome
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles

Retraction: Novel splicing variant c. 208+2T>C in BBS5 segregates with Bardet-Biedl syndrome in an Iranian family by targeted exome sequencing

Journal: Bioscience Reports
Biosci Rep (2024) 44 (10): BSR-2018-1544_RET.
https://doi.org/10.1042/BSR-2018-1544_RET
Published: 07 October 2024
... © 2024 The Author(s). 2024 This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . Bardet-Biedl syndrome BBS5 gene Splicing variant Targeted exome sequencing...
View article titled, Retraction: Novel splicing variant c. 208+2T&amp;gt;C in BBS5 segregates with <span class="search-highlight">Bardet</span>-<span class="search-highlight">Biedl</span> <span class="search-highlight">syndrome</span> in an Iranian family by targeted exome sequencing
Open the PDF for Retraction: Novel splicing variant c. 208+2T&gt;C in BBS5 segregates with <span class="search-highlight">Bardet</span>-<span class="search-highlight">Biedl</span> <span class="search-highlight">syndrome</span> in an Iranian family by targeted exome sequencing in another window
Articles

Novel splicing variant c. 208+2T>C in BBS5 segregates with Bardet–Biedl syndrome in an Iranian family by targeted exome sequencing

Saber Imani, Jingliang Cheng, Jiewen Fu, Abdolkarim Mobasher-Jannat, Chunli Wei, Saman Mohazzab-Torabi, Khosrow Jadidi, Mohammad Hossein Khosravi, Marzieh Dehghan Shasaltaneh, Lisha Yang, Md. Asaduzzaman Khan, Junjiang Fu
Journal: Bioscience Reports
Biosci Rep (2019) 39 (3): BSR20181544.
https://doi.org/10.1042/BSR20181544
Published: 29 March 2019
...Saber Imani; Jingliang Cheng; Jiewen Fu; Abdolkarim Mobasher-Jannat; Chunli Wei; Saman Mohazzab-Torabi; Khosrow Jadidi; Mohammad Hossein Khosravi; Marzieh Dehghan Shasaltaneh; Lisha Yang; Md. Asaduzzaman Khan; Junjiang Fu Bardet–Biedl syndrome (BBS) is a rare genetically heterogeneous ciliopathy...
View article titled, Novel splicing variant c. 208+2T&amp;gt;C in BBS5 segregates with <span class="search-highlight">Bardet</span>–<span class="search-highlight">Biedl</span> <span class="search-highlight">syndrome</span> in an Iranian family by targeted exome sequencing
Open the PDF for Novel splicing variant c. 208+2T&gt;C in BBS5 segregates with <span class="search-highlight">Bardet</span>–<span class="search-highlight">Biedl</span> <span class="search-highlight">syndrome</span> in an Iranian family by targeted exome sequencing in another window
Includes: Supplementary data