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Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fe4c71d0a774413c9e22a650a5cb7776

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

About this item

Full title

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

Publisher

Switzerland: Frontiers Research Foundation

Journal title

Frontiers in molecular neuroscience, 2021-08, Vol.14, p.721047-721047

Language

English

Formats

Publication information

Publisher

Switzerland: Frontiers Research Foundation

More information

Scope and Contents

Contents

Primary lateral sclerosis (PLS) is a progressive upper motor neuron (UMN) disorder. It is debated whether PLS is part of the amyotrophic lateral sclerosis (ALS) spectrum, or a syndrome encompassing different neurodegenerative diseases. Recently, new diagnostic criteria for PLS have been proposed. We describe four patients of two pedigrees, meeting...

Alternative Titles

Full title

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_fe4c71d0a774413c9e22a650a5cb7776

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fe4c71d0a774413c9e22a650a5cb7776

Other Identifiers

ISSN

1662-5099

E-ISSN

1662-5099

DOI

10.3389/fnmol.2021.721047

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