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Uncovering Deletion/Insertion Mutations in Veno-Occlusive Disease with Immunodeficiency Syndrome in An Iranian Family: A Case Report.

Year: 2024
Type: article
Abstract: gene, this study aimed to expedite diagnosis by creating a comprehensive panel for VODI syndrome.
Source: PubMed
Language: English
Subfield: Immunology
Open Access status: green
OpenAlex ID: W4403283840
FWCI:
Cites:
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Related to: 10