Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N Brouwers, K Nuytemans, J van der Zee… - Archives of …, 2007 - jamanetwork.com
Background Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …
被引用次数：154 相关文章

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N Brouwers, K Nuytemans… - Archives of …, 2007 - pubmed.ncbi.nlm.nih.gov
Background Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …

[引用][C] Alzheimer and parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N BROUWERS, K NUYTEMANS… - Archives of …, 2007 - pascal-francis.inist.fr
Alzheimer and parkinson diagnoses in progranulin null mutation carriers in an extended
founder family CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic …

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

N Brouwers, K Nuytemans, J van der Zee… - Archives of …, 2007 - europepmc.org
Background Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N Brouwers, K Nuytemans, J van der Zee… - Archives of …, 2007 - researchportal.vub.be
BACKGROUND: Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …

Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N Brouwers, K Nuytemans, J van der Zee… - ARCHIVES OF …, 2007 - lib.ugent.be
Background: Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …

[引用][C] Alzheimer and parkinson diagnoses in progranulin null mutation carriers in an extended founder family

N BROUWERS, K NUYTEMANS… - Archives of …, 2007 - scholarship.miami.edu
Neurology Biological and medical sciences Medical sciences Diseases of striated muscles.
Neuromuscular diseases Degenerative and inherited degenerative diseases of the nervous …
[PDF] researchgate.net

[PDF][PDF] Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family

Arch Neurol, 2007 - researchgate.net
Background: Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …
[PDF] archive.org

[PDF][PDF] Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family

Arch Neurol, 2007 - scholar.archive.org
Background: Progranulin gene (PGRN) haploinsufficiency was recently associated with
ubiquitin-positive frontotemporal lobar degeneration linked to chromosome 17q21 (FTLDU …

[引用][C] Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family

N Brouwers, K Nuytemans, J van der Zee… - Archives of …, 2007 - cir.nii.ac.jp
Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended
Founder Family | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ …