Publications by authors named "Vera Ancona"

Defects in are associated with either epileptic phenotypes or a spastic paraplegia subtype known as SPG77. Here, we describe an 8-year-old patient with severe and complicated spastic paraplegia, carrying a missense variant (p.Pro361Leu) and a novel intragenic deletion in Of note, the disease is unexpectedly progressing rapidly and in a biphasic way differently from the previously reported cases.

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