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Q41295377-074AFE09-F8C0-4A75-8EE6-AA1A9C155EDC
Q41295377-074AFE09-F8C0-4A75-8EE6-AA1A9C155EDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41295377-074AFE09-F8C0-4A75-8EE6-AA1A9C155EDC
A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease.
P2860
Q41295377-074AFE09-F8C0-4A75-8EE6-AA1A9C155EDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41295377-074AFE09-F8C0-4A75-8EE6-AA1A9C155EDC
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type
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wasDerivedFrom
f28aaf90beec9f71ef7849c3a812a26c5ef16a4c
P2860
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.