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

詳細情報 詳細情報について

• 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

• データソース種別

  • Crossref