Associated Papers
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
Cousin MA et al.
Nature Genetics, 2021
34211179 (PubMed )
Supplement: NIHMS1704971-supplement-Supplementary_Information.pdf
Genomic and Transcriptomic Characterization of Relapsed SCLC Through Rapid Research Autopsy.
Chen HZ et al.
Jto Clinical and Research Reports, 2021
34590014 (PubMed )
Supplement: mmc6.xlsx › T4
Select a paper to view details