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Q43169543-31A1FDA4-26B9-45FA-BFEF-8B7A0119F680
Q43169543-31A1FDA4-26B9-45FA-BFEF-8B7A0119F680
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Statement
http://www.wikidata.org/entity/statement/Q43169543-31A1FDA4-26B9-45FA-BFEF-8B7A0119F680
Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.
P2860
Q43169543-31A1FDA4-26B9-45FA-BFEF-8B7A0119F680
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43169543-31A1FDA4-26B9-45FA-BFEF-8B7A0119F680
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Statement
wasDerivedFrom
a7db8c216510c879460b5a7f23f795a0dbfb5488
P2860
Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1.