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Q34469801-063E4A90-24B4-42EA-9D39-92B8A50D90C3
Q34469801-063E4A90-24B4-42EA-9D39-92B8A50D90C3
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Statement
http://www.wikidata.org/entity/statement/Q34469801-063E4A90-24B4-42EA-9D39-92B8A50D90C3
Fibrillin-1 mutations causing Weill-Marchesani syndrome and acromicric and geleophysic dysplasias disrupt heparan sulfate interactions
P2860
Q34469801-063E4A90-24B4-42EA-9D39-92B8A50D90C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34469801-063E4A90-24B4-42EA-9D39-92B8A50D90C3
rank
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type
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wasDerivedFrom
6352b52eb561479fca8a5f4b7944b2dac7627d89
P2860
Fibrillin-1 and -2 contain heparin-binding sites important for matrix deposition and that support cell attachment.