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Q38880902-4E6871CD-6409-4130-83C5-6C8B7FCEFEB3
Q38880902-4E6871CD-6409-4130-83C5-6C8B7FCEFEB3
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Statement
http://www.wikidata.org/entity/statement/Q38880902-4E6871CD-6409-4130-83C5-6C8B7FCEFEB3
Identification of a PRX variant in a Chinese family with congenital cataract by exome sequencing.
P2860
Q38880902-4E6871CD-6409-4130-83C5-6C8B7FCEFEB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38880902-4E6871CD-6409-4130-83C5-6C8B7FCEFEB3
rank
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Statement
wasDerivedFrom
4c615d85e89f97833cb4eb961aa248cde4d79699
P2860
Periaxin mutations cause recessive Dejerine-Sottas neuropathy.