Novel ferritin L-chain gene variant in a case of hereditary hyperferritinemia-cataract syndrome without family history
Year: 2025
Type: article
Study design: Case Report
Source: Ophthalmic Genetics
Author: Murat Erdogan
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W4407869307