Associated Papers
Novel blended SNRPE-related spliceosomopathy phenotype characterized by microcephaly and congenital atrichia.
Amudhavalli SM et al.
American Journal of Medical Genetics. Part A, 2023
Emerging roles of spliceosome in cancer and immunity.
Yang H et al.
Protein & Cell, 2022
Additional causal SNRPE mutations in hereditary hypotrichosis simplex.
Pan C et al.
The British Journal of Dermatology, 2021
A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.
Chen T et al.
Plos Genetics, 2019
Genetics of human isolated hereditary hair loss disorders.
Basit S et al.
Clinical Genetics, 2015
MitoFates: improved prediction of mitochondrial targeting sequences and their cleavage sites.
Fukasawa Y et al.
Molecular & Cellular Proteomics : Mcp, 2015
25670805 (PubMed )
Supplement: supp_M114.043083_mcp.M114.043083-16.xlsx › TableS9B
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.
Pasternack SM et al.
American Journal of Human Genetics, 2013
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