Fig. 2From: A novel p.A191D matrilin-3 variant in a Vietnamese family with multiple epiphyseal dysplasia: a case reportIdentification of a novel de novo missense variant in MATN3 (a) The DNA-sequence electropherogram of parents and brothercompared with that of patient. A heterozygousmissense variant (c.572C > A; p.A191D) in exon 2 of the MATN3 was identified. (b) The variant is evolutionarily conservedBack to article page