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Atypical fundoscopic manifestation with good visual prognosis in familial hypomagnesemia with hypercalciuria and nephrocalcinosis

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Year: 2024
Type: article
Study design: Case Report
Source: Ophthalmic Genetics
DOI: 10.1080/13816810.2024.2390021
Authors: M. Girón-Ortega, M. J. Morillo Sánchez, M. Soto-Sierra, M. Mena, G. Antinolo, M. Ramos-Jiménez, M. López-Domínguez, E. Rodríguez-de-la-Rúa
Institutions: Hospital Universitario Virgen Macarena, Consejo Superior de Investigaciones Científicas, Centre for Biomedical Network Research on Rare Diseases, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Instituto de Salud Carlos III
Language: English

Topic: Retinal Development and Disorders
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Instituto de Salud Carlos III
OpenAlex ID: W4402007210
FWCI:
Cites: 18
Cited by:
Related to: 10
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