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Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34).
Abraham, Reema Miria; Viswanathan, Ganesh Kumar; Dass, Jasmita; Dhawan, Rishi; Aggarwal, Mukul; Kumar, Pradeep; Seth, Tulika; Mahapatra, Manoranjan.
Afiliação
  • Abraham RM; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Viswanathan GK; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Dass J; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Dhawan R; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Aggarwal M; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Kumar P; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Seth T; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
  • Mahapatra M; Department of Hematology, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Int J Lab Hematol ; 44(3): e132-e134, 2022 06.
Article em En | MEDLINE | ID: mdl-34847617

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Pré-Calicreína Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Pré-Calicreína Idioma: En Ano de publicação: 2022 Tipo de documento: Article