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Volumn 345, Issue 5, 2001, Pages 325-334
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Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
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Author keywords
[No Author keywords available]
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Indexed keywords
ACTIVIN RECEPTOR;
ACTIVIN RECEPTOR LIKE KINASE 1;
BONE MORPHOGENETIC PROTEIN 2;
BONE MORPHOGENETIC PROTEIN RECEPTOR;
ENDOGLIN;
TRANSFORMING GROWTH FACTOR BETA;
TRANSFORMING GROWTH FACTOR BETA RECEPTOR;
UNCLASSIFIED DRUG;
ADULT;
ARTICLE;
CHILD;
CHROMOSOME 12Q;
CLINICAL ARTICLE;
CLINICAL FEATURE;
FAMILY STUDY;
FEMALE;
GENETIC ANALYSIS;
GENETIC LINKAGE;
HUMAN;
IMMUNOHISTOCHEMISTRY;
MALE;
MOLECULAR GENETICS;
PRIORITY JOURNAL;
PULMONARY HYPERTENSION;
RENDU OSLER WEBER DISEASE;
VASODILATATION;
ACTIVIN RECEPTORS;
ADULT;
BONE MORPHOGENETIC PROTEIN RECEPTORS, TYPE II;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 12;
FEMALE;
HUMANS;
HYPERTENSION, PULMONARY;
LUNG;
MALE;
MICROSATELLITE REPEATS;
MIDDLE AGED;
MUTATION;
MUTATION, MISSENSE;
PEDIGREE;
PROTEIN-SERINE-THREONINE KINASES;
SIGNAL TRANSDUCTION;
TELANGIECTASIA, HEREDITARY HEMORRHAGIC;
TRANSFORMING GROWTH FACTOR BETA;
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EID: 0035797556
PISSN: 00284793
EISSN: None
Source Type: Journal
DOI: 10.1056/NEJM200108023450503 Document Type: Article |
Times cited : (624)
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References (33)
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