Additional file 2: Table S1. of Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review

Andreas Puschmann (139501); Christer Nilsson (139506); Danielle van Westen (56857); Elisabet Englund (377839); Emil Ygland (4799424); Irina Alafuzoff (163896); Karin Nilsson (281963); Lars Gustafson (4799421); Maria Landqvist WaldĂś (4799433); Oskar Hansson (233854); Rosa Rademakers (85403); Zbigniew Wszolek (213912)

Additional file 2: Table S1. of Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review

Authors: Andreas Puschmann (139501)
Christer Nilsson (139506)
Danielle van Westen (56857)
Elisabet Englund (377839)
Emil Ygland (4799424)
Irina Alafuzoff (163896)
Karin Nilsson (281963)
Lars Gustafson (4799421)
Maria Landqvist WaldĂś (4799433)
Oskar Hansson (233854)
Rosa Rademakers (85403)
Zbigniew Wszolek (213912)
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Doi

Abstract

MAPT haplotype determination based on exome sequencing data. Individuals, residues, and haplotype as indicated. Note that the proband, individual III-2, had Alzheimerâs disease and was excluded from the study. (PDF 181 kb

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