TY  - GEN
AU  - Pece-Barbara,N
AU  - Cymerman,U
AU  - Vera,S
AU  - Marchuk,D A
AU  - Letarte,M
TI  - Expression analysis of four endoglin missense mutations suggests that haploinsufficiency is the predominant mechanism for hereditary hemorrhagic telangiectasia type 1
SN  - 0964-6906
PY  - 1999///1214
KW  - Animals
KW  - Antigens, CD
KW  - Base Sequence
KW  - COS Cells
KW  - Cell Line
KW  - Cell Membrane
KW  - metabolism
KW  - DNA Primers
KW  - Endoglin
KW  - Haplotypes
KW  - Humans
KW  - Mutation, Missense
KW  - Receptors, Cell Surface
KW  - Telangiectasia, Hereditary Hemorrhagic
KW  - genetics
KW  - Vascular Cell Adhesion Molecule-1
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/hmg/8.12.2171
ER  -