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Q33618805-3CCF21F3-A89F-46B5-99AC-69FDF4C6C852
Q33618805-3CCF21F3-A89F-46B5-99AC-69FDF4C6C852
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http://www.wikidata.org/entity/statement/Q33618805-3CCF21F3-A89F-46B5-99AC-69FDF4C6C852
Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
P2860
Q33618805-3CCF21F3-A89F-46B5-99AC-69FDF4C6C852
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33618805-3CCF21F3-A89F-46B5-99AC-69FDF4C6C852
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1e922a9105d6c120364aeab2fc78cbb4ec825777
P2860
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.