New variant in KITLG shapes the pathogenesis of familial progressive hyper- and hypo-pigmentation
Fields of Study & Subjects
Genetic and rare skin diseases.
RNA regulation and disease
melanin and skin pigmentation
Publication details
- Journal / source
- Molecular Genetics and Genomics
- Publisher
- Springer Science and Business Media LLC
- Volume
- 301
- Issue
- 1
- Publication date
- 4 March 2026
- Language
- EN