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Q37363942-1BF3E84D-9770-4035-92FF-88E4EC75A5DD
Q37363942-1BF3E84D-9770-4035-92FF-88E4EC75A5DD
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Statement
http://www.wikidata.org/entity/statement/Q37363942-1BF3E84D-9770-4035-92FF-88E4EC75A5DD
Two novel PRP31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa.
P2860
Q37363942-1BF3E84D-9770-4035-92FF-88E4EC75A5DD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37363942-1BF3E84D-9770-4035-92FF-88E4EC75A5DD
rank
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type
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Statement
wasDerivedFrom
a55d6eea3d44bd12253d02fedac4b5f5e13430bd
P2860
A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosa.