M L Katz et al.
Mammalian genome : official journal of the International Mammalian Genome Society, 10(11), 1050-1053 (1999-11-11)
Late-infantile ceroid-lipofuscinosis (CLN2) is an autosomal recessively inherited, neurodegenerative disease in humans. The CLN2 locus has been mapped to Chromosome (Chr) 11p15, and its sequence and genomic organization have recently been reported. In the present study, the cDNA sequence, exon/intron