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pro vyhledávání: '"Guilherme Mitne"'
Autor:
Alessandra Starling, Fernando Kok, Mayana Zatz, Guilherme Mitne, Marcilia Martyn, A Cerqueira, M. Valadares, Zodja Graciani, Carlos Bandeira de Mello Monteiro, Miguel Mitne-Neto, Thomas Deufel, André Pessoa, Christian Beetz, Paulo Hubert, Clarissa Bueno, Anders O H Nygren
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
SPG4 mutations are the most frequent cause of autosomal-dominant hereditary spastic paraplegia (HSP). SPG4 HSP is characterized by large inter- and intrafamilial variability in age at onset (AAO) and disease severity. The broad spectrum of SPG4 mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e372ef60cbbf94fe7fff0bc7bbe0e950