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Q33845359-BE0A1B0D-D3A8-42D6-B6AB-067BDD471562
Q33845359-BE0A1B0D-D3A8-42D6-B6AB-067BDD471562
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http://www.wikidata.org/entity/statement/Q33845359-BE0A1B0D-D3A8-42D6-B6AB-067BDD471562
Mutations in ASCC3L1 on 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese family.
P2860
Q33845359-BE0A1B0D-D3A8-42D6-B6AB-067BDD471562
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33845359-BE0A1B0D-D3A8-42D6-B6AB-067BDD471562
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wasDerivedFrom
7c8e9e2f7e62d5d2e6db754b5bd6320d4c719d9b
P2860
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy