A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene-Reference-Cited by-同舟云学术

A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene

Published:2021-10 Issue: Volume:106 Page:343.e1-343.e8
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Olszewska Diana A.,Fearon Conor^ORCID,McGuigan Christopher,McVeigh Terri P^ORCID,Houlden Henry,Polke James M^ORCID,Lawlor Brian,Coen Robert,Hutchinson Michael^ORCID,Hutton Michael,Beausang Alan^ORCID,Delon Isabelle^ORCID,Brett Francesca,Sevastou Ioanna,Seto-Salvia Nuria,de Silva Rohan,Lynch Tim^ORCID

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference40 articles.

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