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SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil
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Published in: | Clinical genetics 2014-08, Vol.86 (2), p.194-196 |
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cites | cdi_FETCH-LOGICAL-c4572-b6b987dc8d4a63ece86cbd286b3e1c3623c6efc571f71414f8c48045a854dd523 |
container_end_page | 196 |
container_issue | 2 |
container_start_page | 194 |
container_title | Clinical genetics |
container_volume | 86 |
creator | França Jr, M.C. Dogini, D.B. D'Abreu, A. Teive, H.A.G. Munhoz, R.P. Raskin, S. Moro, A. Melo, C.C. Gomes, A.P. Saute, J.A.M. Jardim, L.B. Lopes-Cendes, I. |
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doi_str_mv | 10.1111/cge.12252 |
format | article |
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language | eng |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | Adenosine Triphosphatases - genetics Base Sequence Brazil DNA Mutational Analysis Exons - genetics Family Genes, Dominant Humans Molecular Sequence Data Mutation - genetics Mutation Rate Spastic Paraplegia, Hereditary - genetics Spastin |
title | SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil |
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