Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families.

Amjad Ali, Abdullah,Muhammad Bilal,Emily Kathryn Mis,Saquib Ali Lakhani,Wasim Ahmad,Imran Ullah

Molecular biology reports（2023）

引用 0|浏览2

暂无评分

摘要

The study not only expanded mutations spectrum in the BBS genes, but this will facilitate diagnosis and genetic counselling of families carrying BBS related phenotypes in Pakistani population.

查看译文

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要