(Q40920042)
Statements
1 reference
Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1. (English)
1 reference
N Pece-Barbara
1 reference
U Cymerman
1 reference
S Vera
1 reference
D A Marchuk
1 reference
M Letarte
1 reference
1 November 1999
1 reference
1 reference
8
1 reference
12
1 reference
2171-2181
1 reference
Identifiers
1 reference
1 reference