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...

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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

Internet

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

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