(Q30583835)

19 October 2017

Exome sequencing in familial corticobasal degeneration (English)

1 reference

corticobasal degeneration

19 October 2017

1 reference

1

1 reference

19 October 2017

Matthew Bainbridge

2

1 reference

19 October 2017

Jose Fidel Baizabal-Carvallo

3

1 reference

19 October 2017

Andreana Rivera

4

1 reference

19 October 2017

Bradley Miller

5

1 reference

19 October 2017

Peicheng Du

6

1 reference

19 October 2017

Vladyslav Kholodovych

7

1 reference

19 October 2017

Suzanne Powell

8

1 reference

19 October 2017

William Ondo

9

1 reference

19 October 2017

16 July 2013

1 reference

Parkinsonism and Related Disorders

19 October 2017

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

19 October 2017

19

1 reference

19 October 2017

11

1 reference

19 October 2017

1049-1052

1 reference

Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities

19 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Whole exome capture in solution with 3 Gbp of data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Fast and accurate short read alignment with Burrows-Wheeler transform

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Parkinsonism, Lrrk2 G2019S, and tau neuropathology

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Diagnostic criteria for corticobasal syndrome: a comparative study.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

A case of clinically and neuropathologically atypical corticobasal degeneration with widespread iron deposition

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

The eye of the tiger sign in cortical-basal ganglionic degeneration

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4100470

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23867865

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.PARKRELDIS.2013.06.016

1 reference

19 October 2017

1 reference

19 October 2017

PubMed publication ID

23867865

1 reference