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Subject ABCA4 -- CLRN1 -- Exome sequencing -- Inherited retinal dystrophy

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
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