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Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing
by
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
Published in
Molecular genetics & genomic medicine
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Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies
by
Azab, Belal
,
Barham, Raghda
,
Ali, Dema
,
Dardas, Zain
,
Rashdan, Lana
,
Bijawi, Maysa
,
Maswadi, Ranad
,
Awidi, Abdelhalim
,
Jafar, Hanan
,
Abu-Ameerh, Mohammed
,
Al-Bdour, Muawyah
,
Amr, Sami
,
Awidi, Abdalla
Published in
Canadian journal of ophthalmology
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Canadian Journal Of Ophthalmology
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Molecular Genetics & Genomic Medicine
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Life Sciences & Biomedicine
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Science & Technology
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Abca4
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Adult
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Analysis
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Atp-Binding Cassette Transporters - Genetics
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Audiometry
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Child
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Clrn1
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Deoxyribonucleic Acid
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Disease
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Dna
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Dna Sequencing
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Exome
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Exome Sequencing
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Female
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