retinitis pigmentosa type 30 (RP30)
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Contents
1
Genetics
2
More general terms
3
References
4
Database
Genetics
autosomal dominant
associated with defects in
FSCN2
gene
More general terms
retinitis pigmentosa (RP)
References
↑
OMIM
https://mirror.omim.org/entry/607921
Database
OMIM:
https://mirror.omim.org/entry/607921
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