HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of …
Objective Familial autosomal dominant frontotemporal dementia with ubiquitin‐positive, tau‐
negative inclusions in the brain linked to 17q21‐22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21‐22 recently has been reported to carry null …
[PDF][PDF] HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide …
A Neurol - Ann Neurol, 2006 - researchgate.net
Objective—Familial autosomal dominant frontotemporal dementia with ubiquitin-positive,
taunegative inclusions in the brain linked to 17q21-22 recently has been reported to carry …
taunegative inclusions in the brain linked to 17q21-22 recently has been reported to carry …
[PDF][PDF] HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide …
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty… - Ann Neurol, 2006 - bib.irb.hr
Objective: Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of …
O Mukherjee, P Pastor, NJ Cairns… - Annals of …, 2006 - europepmc.org
Objective Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
[引用][C] HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of …
O MUKHERJEE, P PASTOR, D LEVITCH… - Annals of …, 2006 - pascal-francis.inist.fr
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative
inclusions caused by a missense mutation in the signal peptide of progranulin CNRS Inist …
inclusions caused by a missense mutation in the signal peptide of progranulin CNRS Inist …
[PDF][PDF] HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide …
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty… - Ann Neurol, 2006 - 161.53.22.65
Objective: Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
[PDF][PDF] HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide …
O Mukherjee, P Pastor, NJ Cairns… - Ann …, 2006 - brightspotcdn.byu.edu
Objective: Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
[HTML][HTML] HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal …
O Mukherjee, P Pastor, NJ Cairns… - Annals of …, 2006 - ncbi.nlm.nih.gov
Objective Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
[引用][C] HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of …
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty… - Annals of …, 2006 - cir.nii.ac.jp
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative
inclusions caused by a missense mutation in the signal peptide of progranulin | CiNii Research …
inclusions caused by a missense mutation in the signal peptide of progranulin | CiNii Research …
HDDD2 Is a Familial Frontotemporal Lobar Degeneration with Ubiquitin-Positive, Tau-Negative Inclusions Caused by a Missense Mutation in the Signal Peptide of …
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty… - Annals of neurology, 2006 - croris.hr
Objective Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …
negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null …