1. Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. Issue 3 (22nd January 2020) Authors: Abu‐Ameerh, Mohammed; Mohammad, Hashim; Dardas, Zain; Barham, Raghda; Ali, Dema; Bijawi, Maysa; Tawalbeh, Mohamed; Amr, Sami; Hatmal, Ma'mon M.; Al‐Bdour, Muawyah; Awidi, Abdalla; Azab, Belal Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 3(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗