CV Lattes
Universidade Estadual de Campinas (UNICAMP). Faculdade de Ciências Médicas (FCM) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduate in Medicine at Universidade Federal do Paraná (1992), master's in Genetics at Universidade Estadual de Campinas (1998) and ph.d. in Genetics at Universidade Estadual de Campinas (2002). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: clinical genetics, genodermatosis, inborn errors of metabolism, dysmorphology, and mental retardation. (Source: Lattes Curriculum)
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GM1 gangliosidosis is a rare autosomal disease caused by the deficiency of lysosomal enzyme ²-galactosidase, which is coded by the GLB1 gene. The enzimatic activity decrease leads to GM1 and GA1 gangliosides deposition inside the lysosomes. The disease is classified in three clinical types according to age of onset, enzymatic activity and severity. The Danio rerio (zebrafish) is an inter…
| 4 / 3 | Completed research grants |
| 2 / 0 | Completed scholarships in Brazil |
| 6 / 3 | All research grants and scholarships |
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