Skip to Main Content

Paper Details

Pathway-driven rare germline variants associated with transplant-associated thrombotic microangiopathy (TA-TMA).
Thromb Res
1
2023
189 functional rare variants, ADAMTS13, LRP1, TA-TMA, VWF, endothelial, germline, patients, rare germline variants, rare variants, transplant-associated thrombotic microangiopathy, von Willebrand, von Willebrand factor
Author NameAffiliation
Christopher I AmosInstitute for Clinical & Translational Research, Baylor College of Medicine
Christopher I AmosInstitute for Clinical & Translational Research, Baylor College of Medicine
Chao ChengInstitute for Clinical & Translational Research, Baylor College of Medicine
Chao ChengInstitute for Clinical & Translational Research, Baylor College of Medicine
Pavan K BhatrajuUniversity of Washington School of Medicine
  • 1 - 5

Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink