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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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| Autori principali: | , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Lippincott Williams & Wilkins
2012
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| Soggetti: | |
| Accesso online: | 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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