A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1
Year: 2024
Type: article
Authors: Gou Y, Wang P, Yang W, Feng Y, Peng X, Liu H, Liu S, Zhang X
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W7008592189
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