A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review
Crossref DOI link: https://doi.org/10.1186/s12883-017-0959-2
Published Online: 2017-09-15
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Hosaka, Takashi
Ishii, Kazuhiro
Miura, Takeshi
Mezaki, Naomi
Kasuga, Kensaku
Ikeuchi, Takeshi
Tamaoka, Akira
Funding for this research was provided by:
Japan Agency for Medical Research and Development (JP)