Subtle neuropsychiatric and neurocognitive changes in hereditary gelsolin amyloidosis (AGel amyloidosis)

Hereditary gelsolin amyloidosis (AGel amyloidosis) is an autosomal dominant form of systemic amyloidosis caused by a c.640G>A or c.640G>T mutation in the gene coding for gelsolin. Principal clinical manifestations include corneal lattice dystrophy, cranial neuropathy and cutis laxa with vascul...

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Detalles Bibliográficos
Autores principales: Kantanen, Mari, Kiuru-Enari, Sari, Salonen, Oili, Kaipainen, Markku, Hokkanen, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2014
Materias:
Cognitive Disorders
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121541/
https://www.ncbi.nlm.nih.gov/pubmed/25097823
http://dx.doi.org/10.7717/peerj.493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121541/
https://www.ncbi.nlm.nih.gov/pubmed/25097823
http://dx.doi.org/10.7717/peerj.493

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