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Stuart Gillies
Stuart Gillies
St Mary's Hospital
Missense mutation
Exome
GUCY2D
CERKL Gene
Compound heterozygosity
1
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14
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A founder mutation in CERKL is a major cause of retinal dystrophy in Finland.
2018
Acta Ophthalmologica
Kristiina Avela
Eeva-Marja Sankila
Sanna Seitsonen
Liina Kuuluvainen
Stephanie Barton
Stuart Gillies
Kristiina Aittomäki
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Citations (14)
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