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612862.2.1
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Subject Details
Country
Morocco
HPO Terms
Visual impairment; Rod-cone dystrophy; Nyctalopia;
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Sex
Female
Family History
Yes
Parental Consanguinity
Yes
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_006343.3:c.2323C>T
2
Retinitis Pigmentosa 38
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References
Ksantini et al, 2012
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