Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation

DOI Web Site Web Site 1 Citations

Journal

Neurobiology of Aging

Neurobiology of Aging 41 200.e1-200.e5, 2016-05

Elsevier BV

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CRID

1360298760595753216
DOI

10.1016/j.neurobiolaging.2016.02.019
ISSN

01974580
Web Site

https://api.elsevier.com/content/article/PII:S0197458016001780?httpAccept=text/xml

https://api.elsevier.com/content/article/PII:S0197458016001780?httpAccept=text/plain
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