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248200.2
Home
Subject Details
Country
Lebanon
HPO Terms
Blindness
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Sex
Unknown
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_000350.3:c.1648G>A
2
Stargardt Disease 1
Download Table
References
Jalkh et al. 2019
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