L. Ieno

Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy.

F. Contaldo, F. Pasanisi, P. Buono, 2005, Clinical chemistry.

Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion

L. Vitagliano, A. Zagari, F. Salvatore, 2010, Human mutation.

Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosis

F. Paparo, L. Giordano, A. Viola, 2007, The British journal of dermatology.

Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene

L. Vitagliano, A. Zagari, F. Salvatore, 2004, Human mutation.