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

MR Almeida, MC Macário, L Ramos, I Baldeiras… - Neurobiology of …, 2016 - Elsevier
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …
被引用次数：114 相关文章

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

MR Almeida, MC Macário, L Ramos… - Neurobiology of …, 2016 - europepmc.org
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …

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

MR Almeida, MC Macário, L Ramos… - Neurobiology of …, 2016 - pubmed.ncbi.nlm.nih.gov
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …

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

MR Almeida, MC Macário, L Ramos, I Baldeiras… - Neurobiology of …, 2016 - infona.pl
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …

[引用][C] Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene …

MR Almeida, MC Macário, L Ramos, I Baldeiras… - Neurobiology of …, 2016 - cir.nii.ac.jp
Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal
ceroid lipofuscinosis phenotypes due to progranulin gene mutation | CiNii Research CiNii 国立 …

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

MR Almeida, MC Macário, L Ramos, I Baldeiras… - Neurobiology of …, 2016 - infona.pl
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …