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Wiley, Human Mutation: Variation, Informatics and Disease, 1(41), p. 169-181, 2019
DOI: 10.1002/humu.23904
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A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2
Journal article published in 2019 by
Meliha Karsak,
Konstantin Glebov,
Marina Scheffold,
Thomas Bajaj,
Amit Kawalia,
Ilker Karaca,
Sebastian Rading,
Johannes Kornhuber,
Oliver Peters,
Monica Diez‐Fairen,
Lutz Frölich,
Michael Hüll,
Jens Wiltfang 
,
Martin Scherer,
Steffi Riedel‐Heller
and other authors.
,
Martin Scherer,
Steffi Riedel‐Heller
and other authors.
This paper is made freely available by the publisher.
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