Novel splicing variant c. 208+2TC in BBS5 segregates with Bardet–Biedl syndrome in an Iranian family...
<jats:title>Abstract</jats:title> <jats:p>Bardet–Biedl syndrome (BBS) is a rare genetically heterogeneous ciliopathy which accompanies retinitis pigmentosa (RP). However, the BBS5 mutation remains unclear in Iranians with BBS. The purpose of study is to evaluate gene...
|Journal Title:||Bioscience Reports|
|Authors and Corporations:||, , , , , , , , , , ,|
|In:||Bioscience Reports, 39, 2019, 3|
|Type of Resource:||E-Article|
Portland Press Ltd.