Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations

Congenital mutations of the Wilms' tumor 1 (WT1) gene can lead to various abnormalities, including renal/gonadal developmental disorders and cardiac malformations. Although there have been many reports of somatic WT1 mutations in patients with acute myeloid leukemia and myelodysplastic syndrome...

Descripción completa

Detalles Bibliográficos
Autores principales: Murakami, Ken, Yamaguchi, Yuuta, Kida, Yuko, Morikawa, Yoichiro, Ujiie, Hidetoshi, Sugahara, Hiroyuki, Nannya, Yasuhito, Ogawa, Seishi, Kanakura, Yuzuru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710374/
https://www.ncbi.nlm.nih.gov/pubmed/34053991
http://dx.doi.org/10.2169/internalmedicine.7571-21

Ejemplares similares

Ejemplares similares