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Q46237828-7EA2C770-021C-4271-9279-6D5B8B3A1F28
Q46237828-7EA2C770-021C-4271-9279-6D5B8B3A1F28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46237828-7EA2C770-021C-4271-9279-6D5B8B3A1F28
TBX1 loss-of-function mutation contributes to congenital conotruncal defects.
P2860
Q46237828-7EA2C770-021C-4271-9279-6D5B8B3A1F28
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46237828-7EA2C770-021C-4271-9279-6D5B8B3A1F28
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
8124828c8e4a098ef7dd1fb3dca253d20ff2c01c
P2860
Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion.