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Primary Familial Brain Calcification (Fahr Disease) Due to a Novel Mutation in Solute Carrier 20 A2 Gene

Year: 2026

Type: article

Study design: Case Report

Source: Annals of African Medicine

DOI: 10.4103/aam.aam_319_26

Authors: Somarajan Anandan, Sajeesh S. Rajendran, Joesni Joy, Sreelakshmi Binoy

Language: English

Topic: Neurological diseases and metabolism

Subfield: Neurology

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7166812593

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