Associated Papers
LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy.
Crespin M et al.
Hgg Advances, 2025
Progress in leukodystrophies with zebrafish.
Shih HY et al.
Development, Growth & Differentiation, 2024
Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease.
Derksen A et al.
Hgg Advances, 2021
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 341.162
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