Browsing by Author "Hassan, MJ"
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A 24-generation-old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome
Kaygusuz, Emrah; Khayyat, AIA; Abdullah, U; Budde, BS; Asif, M; Ahmed, I; Makhdoom, EUH; Sur-Erdem, I; Baig, JM; Khan, MMA; Toliat, MR; Becker, C; Anwar, H; Iqbal, M; Fischer, S; Jameel, M; Sher, M; Tariq, M; Malik, NA; Hassan, MJ; Thiele, H; Tinschert, S; Eichinger, L; Höning, S; Baig, SM (Wiley, 2021)Jawad syndrome is a multiple congenital anomaly and intellectual disability syndrome with mutation in RBBP8 reported only in two families. Here, we report on two new families from Pakistan and identified a previously ...