Figure 1
From: Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
Family segregation patterns and mutations detected in the MSMM Family. The family includes two probands (male MSMM001 and female MSMM002), concurrently affected by multiple sclerosis and malignant melanoma. Both probands were homozygous for a rare Gly578Ser predicted pathogenic variant in the NLRP1 gene.
