Yüklüyor......

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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Lippincott Williams & Wilkins 2012
Konular:
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!