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611131.3.1
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Subject Details
Country
Morocco
HPO Terms
Rod-cone dystrophy
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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_014249.4:c.932G>A
2
Retinitis Pigmentosa 37
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References
Bandah et al. 2009
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