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Q37363942-3EB062DC-4834-41F5-9A32-3A7675BF10D8
Q37363942-3EB062DC-4834-41F5-9A32-3A7675BF10D8
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http://www.wikidata.org/entity/statement/Q37363942-3EB062DC-4834-41F5-9A32-3A7675BF10D8
Two novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa.
P2860
Q37363942-3EB062DC-4834-41F5-9A32-3A7675BF10D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37363942-3EB062DC-4834-41F5-9A32-3A7675BF10D8
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wasDerivedFrom
a55d6eea3d44bd12253d02fedac4b5f5e13430bd
P2860
Novel deletion in the pre-mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family