retinitis pigmentosa type 41; retinal degeneration autosomal recessive prominin-related (RP41)
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Contents
1
Genetics
2
More general terms
3
Additional terms
4
References
5
Database
Genetics
associated with defects in
PROM1
More general terms
retinitis pigmentosa (RP)
Additional terms
progressive rod-cone degeneration protein (PRCD)
References
↑
OMIM
https://mirror.omim.org/entry/612095
Database
OMIM:
https://mirror.omim.org/entry/612095
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