Fig. 1From: A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case reportThe family pedigree showing the mutations detected in CLN6. a The pedigree of the family with late infantile neuronal ceroid lipofuscinosis (LINCL). The arrow indicates the proband; his parents have no signs of LINCL. b The mutations detected in the family. The proband is homozygous, while the parents are heterozygousBack to article page