Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin

OBJECTIVE: To report the phenotypic characterization of monozygotic twins with mutations encoding progranulin (PGRN). METHODS: We studied a twin pair with an exon 4 gene deletion in the PGRN gene. Both twins had clinical and neuropsychological examinations as well as structural MRI and fluorodeoxygl...

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Detalhes bibliográficos
Main Authors: McDade, E., Boeve, B.F., Burrus, T.M., Boot, B.P., Kantarci, K., Fields, J., Lowe, V.J., Peller, P., Knopman, D., Baker, M., Finch, N., Rademakers, R., Petersen, R.
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2012
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3324318/
https://ncbi.nlm.nih.gov/pubmed/22491866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e318251594c
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