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Association of Late Onset Spastic Paraparesis and Dementia: Probably an autosomal dominant form of complicated paraplegia Luis Arturo Lizcano Gil, Diana García Cruz, María del P Bernal Beltran … [et.al]

Colaborador(es): Tipo de material: TextoTextoIdioma: Inglés Detalles de publicación: Wiley-Liss; 1997Descripción: 1-6; tabls.; figsTema(s): Resumen: The hereditary paraplegias are a heterogeneous group of genetic disorders characterized mainly by spastic paraparesis, which may be found as an isolated "pure form" known as Strümpell-Lorrain syndrome, or associated with a wide group of other manifestatio
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The hereditary paraplegias are a heterogeneous group of genetic disorders characterized mainly by spastic paraparesis, which may be found as an isolated "pure form" known as Strümpell-Lorrain syndrome, or associated with a wide group of other manifestatio

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