Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
Parra-Perez AM et al.
Medcomm, 2025
40989574 (PubMed )
Supplement: MCO2-6-e70394-s001.xlsx › TableS13
SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
Dardour L et al.
Cold Spring Harbor Molecular Case Studies, 2017
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