Extending the spectrum of CLRN1...

Molecular Genetics & Genomic Medicine 2020 / 01

Extending the spectrum of CLRN1 ‐ and ABCA4 ‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing

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
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Language:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.1123
Date:
January, 2020
File:
PDF, 1.63 MB
english, 2020
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