Recent advances in the genetics of the ALS-FTLD complex (Q38000119)

26 August 2017

Recent advances in the genetics of the ALS-FTLD complex (English)

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amyotrophic lateral sclerosis

26 August 2017

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Huw R Morris

1

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26 August 2017

Adrian J Waite

2

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26 August 2017

Nigel M Williams

3

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26 August 2017

James W Neal

4

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26 August 2017

Derek J Blake

5

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26 August 2017

1 June 2012

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Current Neurology and Neuroscience Reports

26 August 2017

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26 August 2017

12

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26 August 2017

3

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26 August 2017

243-250

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https://scigraph.springernature.com/pub.10.1007/s11910-012-0268-5

26 August 2017

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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

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Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

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Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

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Ubiquilin at a crossroads in protein degradation pathways

21 January 2018

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Ubiquilin functions in autophagy and is degraded by chaperone-mediated autophagy

21 January 2018

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Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

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DOI

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26 August 2017

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