W. Yi

Genotype-phenotype correlations in neuronal ceroid lipofuscinosis due to palmitoyl-protein thioesterase deficiency.

K. Wisniewski, S. Hofmann, A. Das, 1999, Molecular genetics and metabolism.

Molecular genetics of palmitoyl-protein thioesterase deficiency in the U.S.

K. Wisniewski, S. Hofmann, A. Das, 1998, The Journal of clinical investigation.

Structure of the human palmitoyl-protein thioesterase-2 gene (PPT2) in the major histocompatibility complex on chromosome 6p21.3.

S. Hofmann, A. Soyombo, W. Yi, 1999, Genomics.

New mutations genes in the neuronal ceroid lipofuscinosis

P. Taschner, P. Franken, T. Salonen, 2001 .

New mutations in the neuronal ceroid lipofuscinosis genes.

P. Taschner, P. Franken, I. Järvelä, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

cDNA and genomic cloning of human palmitoyl-protein thioesterase (PPT), the enzyme defective in infantile neuronal ceroid lipofuscinosis.

S. Hofmann, W. Yi, J. E. Schriner, 1996, Genomics.

cDNA and Genomic Cloning of Human Palmitoyl-Protein Thioesterase (PPT), the Enzyme Defective in Infantile Neuronal Ceroid Lipofuscinosis: Volume34,Number 3 (1996), pages 317–322:

S. Hofmann, W. Yi, J. E. Schriner, 1996 .