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                                       Details for article 1 of 36 found articles
 
 
  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
 
 
Title: 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
Author: Olszewska, Diana A.
Fearon, Conor
McGuigan, Christopher
McVeigh, Terri P
Houlden, Henry
Polke, James M
Lawlor, Brian
Coen, Robert
Hutchinson, Michael
Hutton, Michael
Beausang, Alan
Delon, Isabelle
Brett, Francesca
Sevastou, Ioanna
Seto-Salvia, Nuria
de Silva, Rohan
Lynch, Tim
Appeared in: Neurobiology of aging
Paging: Volume 106 () nr. C pages 343.e1-343.e8
Year: 2021
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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