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Article

Clinical utility gene card for FRMD7-related infantile nystagmus.

European journal of human genetics : EJHG - 1 Oct 2021

Dawar Basu, Kuht Helen J, Han Jinu, Maconachie Gail D E, Thomas Mervyn G

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Share to Cytoskeletal Proteins
Share to Genetic Diseases, X-Linked
Share to Genetic Testing
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Nystagmus, Congenital

Share to Sensitivity and Specificity

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Identifiers

PMID: 33633368
DOI: 10.1038/s41431-021-00826-9
PMCID: PMC8484540

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