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FBN2

Official Full Name
fibrillin 2
Organism
Homo sapiens
GeneID
2201
Background
The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]
Synonyms
CCA; DA9; EOMD;

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