Associated Papers
Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy.
Ganassi M et al.
Cell Death & Disease, 2026
41611663 (PubMed )
Supplement: 41419_2025_8358_MOESM7_ESM.xlsx › Sheet1
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
Butali A et al.
American Journal of Medical Genetics. Part A, 2013
Structural basis for DNA recognition by the human PAX3 homeodomain.
Birrane G et al.
Biochemistry, 2009
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