Items where Author is "Gellera, C"

Journal article

VERDERIO, E., CAVADINI, P., MONTERMINI, L., WANG, H., LAMANTEA, E., FINOCCHIARO, G., DIDONATO, S., GELLERA, C. and TARONI, F., 1995. Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. Human Molecular Genetics, 4, pp. 19-29.

GELLERA, C., VERDERIO, E., FLORIDIA, G., FINOCCHIARO, G., MONTERMINI, L., CAVADINI, P., ZUFFARDI, O. and TASSE, C., 1994. Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32. Genomics, 24, pp. 195-197.

TARONI, F., VERDERIO, E., FIORUCCI, S., CAVADINI, P., FINOCCHIARO, G., UZIEL, G., LAMANTEA, E., GELLERA, C. and DIDONATO, S., 1992. Molecular characterization of inherited carnitine palmitoyltransferase II deficiency. Proceedings of the National Academy of Sciences of the United States of America, 89, pp. 8429-8433.