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A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome (vol 100, pg 486, 2021)
Journal article   Peer reviewed

A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome (vol 100, pg 486, 2021)

Emrah Kaygusuz, Arwa Ishaq A. Khayyat, Uzma Abdullah, Birgit Susanne Budde, Maria Asif, Ilyas Ahmed, Ehtisham Ul Haq Makhdoom, Ilknur Sur-Erdem, Jamshaid Mahmood Baig, Muhammad Mohsin Ali Khan, …
Clinical genetics, Vol.101(2), pp.272-272
01/02/2022

Abstract

Genetics & Heredity Life Sciences & Biomedicine Science & Technology

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