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Q34342063-5F5D8D4A-E1DC-4B3D-8F93-CB5A18391BCE
Q34342063-5F5D8D4A-E1DC-4B3D-8F93-CB5A18391BCE
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Statement
http://www.wikidata.org/entity/statement/Q34342063-5F5D8D4A-E1DC-4B3D-8F93-CB5A18391BCE
Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta.
P2860
Q34342063-5F5D8D4A-E1DC-4B3D-8F93-CB5A18391BCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34342063-5F5D8D4A-E1DC-4B3D-8F93-CB5A18391BCE
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wasDerivedFrom
d86755a5c5e3be6729814efdbd23c9556ed9af2c
P2860
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)