Associated Papers
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies.
Denisova E et al.
Cancer Gene Therapy, 2022
34045664 (PubMed )
Supplement: 41417_2021_347_MOESM4_ESM.xls › C000-ZZP8UU
Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohort.
Pasqualin LM et al.
Pediatric Neurology, 2014
De novo LMNA mutations cause a new form of congenital muscular dystrophy.
Quijano-Roy S et al.
Annals of Neurology, 2008
Select a paper to view details