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Q36212293-96FBAB63-739B-421A-A110-D52B779AB905
Q36212293-96FBAB63-739B-421A-A110-D52B779AB905
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36212293-96FBAB63-739B-421A-A110-D52B779AB905
Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly
P2860
Q36212293-96FBAB63-739B-421A-A110-D52B779AB905
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36212293-96FBAB63-739B-421A-A110-D52B779AB905
rank
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type
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Statement
wasDerivedFrom
9a8c5ddb03c02ba49d9529cc70093fa76b9fd25d
P2860
The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations.