Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry.

Yenwongfai, Leonard N; Arora, Ranjana; Smith, Alexander P; Kalfa, Theodosia; Husami, Ammar; Radulescu, Vlad; Myers, Kasiani; Lorsbach, Robert

Yenwongfai, Leonard N; Arora, Ranjana; Smith, Alexander P; Kalfa, Theodosia; Husami, Ammar; Radulescu, Vlad; Myers, Kasiani; Lorsbach, Robert.

Afiliación

Yenwongfai LN; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
Arora R; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
Smith AP; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
Kalfa T; Cincinnati Children's, Cincinnati, Ohio, USA.
Husami A; Cincinnati Children's, Cincinnati, Ohio, USA.
Radulescu V; Pediatric Hematology and Oncology, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
Myers K; Cincinnati Children's, Cincinnati, Ohio, USA.
Lorsbach R; Cincinnati Children's, Cincinnati, Ohio, USA.

Pediatr Blood Cancer ; 70(3): e30023, 2023 03.

Article en En | MEDLINE | ID: mdl-36184776

Asunto(s)

Mielofibrosis Primaria; Humanos; Niño; Mielofibrosis Primaria/genética; Mutación; Janus Quinasa 2/genética

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mielofibrosis Primaria Límite: Child / Humans Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

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