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The pheochromocytoma and paraganglioma syndrome: Founder effects and the PGL 1 syndromeOPOCHER, G; BOARETTO, F; PIGNATARO, V et al.Annales d'endocrinologie. 2009, Vol 70, Num 3, pp 157-160, issn 0003-4266, 4 p.Conference Paper

Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosumCRIMELLA, C; ARNOLDI, A; TOSCANO, A et al.Journal of medical genetics. 2009, Vol 46, Num 5, pp 345-351, issn 0022-2593, 7 p.Article

High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasitesMANNO, N; SHERRATT, S; VAZZA, G et al.Carbohydrate polymers. 2014, Vol 113, pp 607-614, issn 0144-8617, 8 p.Article

A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28VAZZA, G; ZORTEA, M; BOARETTO, F et al.American journal of human genetics. 2000, Vol 67, Num 2, pp 504-509, issn 0002-9297Article

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