Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.

Journal of neurology, neurosurgery, and psychiatry - 1 Nov 2009

Rohrer J D, Beck J, Warren J D, King A, Al Sarraj S, Holton J, Revesz T, Collinge J, Mead S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Atrophy
Share to Central Nervous System Diseases
Share to Dementia
Share to Frameshift Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Functional Laterality

Share to Intercellular Signaling Peptides and Proteins

Share to Parkinsonian Disorders

Share to Progranulins

Source

Identifiers

PMID: 19864668
DOI: 10.1136/jnnp.2008.169383

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.PMID 19864668Read ↗

Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation.Semantic proximity Read ↗

Phenotypes and prognosis: clinicopathologic studies of corticobasal degeneration.Semantic proximity Read ↗

A novel deletion in progranulin gene is associated with FTDP-17 and CBSSemantic proximity Read ↗

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.Semantic proximity Read ↗

Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.Semantic proximity Read ↗

Sporadic corticobasal syndrome with progranulin mutation presenting as progressive apraxic agraphia.Semantic proximity Read ↗

Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.Semantic proximity Read ↗

Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation.Semantic proximity Read ↗

Sporadic corticobasal syndrome due to FTLD-TDPSemantic proximity Read ↗

[Abnormal corticogenesis in Marinesco-Sjögren syndrome].Semantic proximity Read ↗

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes.Semantic proximity Read ↗

Phenotypic variability of familial and sporadic Progranulin p.Gln257Profs*27 mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.