Your browser doesn't support javascript.
loading
Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family.
Mustacich, Debbie J; Lai, Li-Wen; Bernas, Michael J; Jones, Jazmine A; Myles, Reginald J; Kuo, Phillip H; Williams, Walter H; Witte, Charles L; Erickson, Robert P; Witte, Marlys Hearst.
Afiliação
  • Mustacich DJ; Department of Surgery, University of Arizona College of Medicine, Tucson.
  • Lai LW; Department of Pathology, University of Arizona College of Medicine, Tucson.
  • Bernas MJ; Department of Surgery, University of Arizona College of Medicine, Tucson.
  • Jones JA; Department of Surgery, University of Arizona College of Medicine, Tucson.
  • Myles RJ; Department of Surgery, University of Arizona College of Medicine, Tucson.
  • Kuo PH; Medical Imaging (Nuclear Medicine), University of Arizona College of Medicine, Tucson.
  • Williams WH; Medical Imaging (Nuclear Medicine), University of Arizona College of Medicine, Tucson.
  • Witte CL; Department of Surgery, University of Arizona College of Medicine, Tucson.
  • Erickson RP; Department of Pediatrics, University of Arizona College of Medicine, Tucson. Electronic address: erickson@peds.arizona.edu.
  • Witte MH; Department of Surgery, University of Arizona College of Medicine, Tucson; Department of Pediatrics, University of Arizona College of Medicine, Tucson. Electronic address: lymph@surgery.arizona.edu.
Am J Med ; 135(2): e31-e41, 2022 02.
Article em En | MEDLINE | ID: mdl-34656527
Assuntos
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Fatores de Transcrição Forkhead / Canais Iônicos / Linfedema Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Am J Med Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Fatores de Transcrição Forkhead / Canais Iônicos / Linfedema Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Am J Med Ano de publicação: 2022 Tipo de documento: Article