Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations. (Q38337400)
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English | Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations. |
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Statements
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations (English)
Louise A Ocaka
Arundhati Dev Borman
Panagiotis I Sergouniotis
Phillip Moradi
Andrew R Webster
Anthony T Moore