Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis

Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis

Blood disorder: Targeted sequencing helps diagnosis when symptoms vary Genetic testing can help accurately diagnose people suspected of having a rare blood disorder called hereditary spherocytosis, the clinical symptoms of which often vary. Researchers in Japan led by Keiko Shimojima Yamamoto from T...

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Bibliographic Details
Main Authors: Keiko Shimojima Yamamoto, Taiju Utshigisawa, Hiromi Ogura, Takako Aoki, Takahiro Kawakami, Shoichi Ohga, Akira Ohara, Etsuro Ito, Toshiyuki Yamamoto, Hitoshi Kanno
Format: Article
Language:English
Published: Nature Publishing Group 2022-01-01
Series:Human Genome Variation
Online Access:https://doi.org/10.1038/s41439-021-00179-1

Internet

https://doi.org/10.1038/s41439-021-00179-1

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