A novel mutation of PKLR gene in a Taiwanese neonate initially presented with severe hemolytic anemia
Saved in:
| Main Authors: | Jen-Yin Hou, Ting-Chi Yeh, Ting-Huan Huang, Pei-Chin Lin, Hsi-Che Liu, Jan-Gowth Chang |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2020-12-01
|
| Series: | Pediatrics and Neonatology |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1875957220301340 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Hemolytic anemia
by: JAMILA ELHOUDZI
Published: (2014-08-01) -
Case report: Identification of a Chinese patient with RAG1 mutations initially presenting as autoimmune hemolytic anemia
by: Xin Chen, et al.
Published: (2024-12-01) -
Congenital hypothyroidism as the initial presentation of pendred syndrome associated with mutated IVS7-2A>G in SLC26A4 gene in a Taiwanese neonate
by: Sun-Mei Chung, et al.
Published: (2023-01-01) -
Ibuprofen-Induced Hemolytic Anemia
by: Aram Barbaryan, et al.
Published: (2013-01-01) -
Spur-Cell Hemolytic Anemia
by: Ayumi Sugiura, et al.
Published: (2024-09-01)