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Q38308028-2519EFD5-D909-481F-BB19-18C9A4B57508
Q38308028-2519EFD5-D909-481F-BB19-18C9A4B57508
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http://www.wikidata.org/entity/statement/Q38308028-2519EFD5-D909-481F-BB19-18C9A4B57508
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.
P2860
Q38308028-2519EFD5-D909-481F-BB19-18C9A4B57508
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38308028-2519EFD5-D909-481F-BB19-18C9A4B57508
rank
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type
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wasDerivedFrom
2fd4d693cd71e5da7aa3d5ff043f5adcf713aecc
P2860
TM14 is a new member of the fibulin family (fibulin-7) that interacts with extracellular matrix molecules and is active for cell binding.