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AIPL1
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Select article: Genome-Wide Homozygosity Mapping in Families with Leber Congenital Amaurosis Identifies Mutations in AIPL1 and RDH12 Genes
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Research article
First published December, 2014
Genome-Wide Homozygosity Mapping in Families with Leber Congenital Amaurosis Identifies Mutations in AIPL1 and RDH12 Genes
Didem Yücel-Yılmaz,
Berçin Tarlan,
Hayyam Kıratlı
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DNA and Cell Biology
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Select article: Leber Congenital Amaurosis: First Genotyped Hungarian Patients and Report of 2 Novel Mutations in the CRB1 and CEP290 Genes
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First published January, 2016
Leber Congenital Amaurosis: First Genotyped Hungarian Patients and Report of 2 Novel Mutations in the CRB1 and CEP290 Genes
Rita Vámos,
Maigi Külm,
Viktoria Szabó
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European Journal of Ophthalmology
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