Open AccessReply: Two heterozygous progranulin mutations in progressive supranuclear palsy
Author(s) -
Vincent Huin,
Mathieu Barbier,
Alexandra Dürr,
Isabelle Le Ber
Publication year - 2020
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awaa456
Subject(s) - missense mutation , progressive supranuclear palsy , compound heterozygosity , phenotype , genetics , mutation , gene , medicine , biology , atrophy
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