A rare heterozygous
 TREM2
 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

M Karsak; K Glebov; M Scheffold; T Bajaj; A Kawalia; I Karaca; S Rading; J Kornhuber; O Peters; M Diez‐Fairen; L Frölich; M Hüll; J Wiltfang; M Scherer; S Riedel‐Heller; A Schneider; MT Heneka; K Fliessbach; A Sharaf; H Thiele; M Lennarz; F Jessen; W Maier; C Kubisch; Z Ignatova; P Nürnberg; P Pastor; J Walter; A Ramirez

doi:10.1002/humu.23904

A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

M Karsak
, K Glebov
, M Scheffold
, T Bajaj
, A Kawalia
, I Karaca
, S Rading
, J Kornhuber
, O Peters
, M Diez‐Fairen
, L Frölich
, M Hüll
, J Wiltfang
, M Scherer
, S Riedel‐Heller
, A Schneider
, MT Heneka
, K Fliessbach
, A Sharaf
, H Thiele

M Lennarz, F Jessen, W Maier, C Kubisch, Z Ignatova, P Nürnberg, P Pastor, J Walter, A Ramirez

Peninsula Medical School

Research output: Contribution to journal › Article › peer-review

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Original language	English
Number of pages	0
Journal	Human Mutation
Volume	0
Issue number	0
DOIs	https://doi.org/10.1002/humu.23904
Publication status	Published - 25 Aug 2019

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10.1002/humu.23904

Karsak et al-2019-Human Mutation

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Karsak, M., Glebov, K., Scheffold, M., Bajaj, T., Kawalia, A., Karaca, I., Rading, S., Kornhuber, J., Peters, O., Diez‐Fairen, M., Frölich, L., Hüll, M., Wiltfang, J., Scherer, M., Riedel‐Heller, S., Schneider, A., Heneka, MT., Fliessbach, K., Sharaf, A., ... Ramirez, A. (2019). A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2. Human Mutation, 0(0). https://doi.org/10.1002/humu.23904

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title = "A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2",

author = "M Karsak and K Glebov and M Scheffold and T Bajaj and A Kawalia and I Karaca and S Rading and J Kornhuber and O Peters and M Diez‐Fairen and L Fr{\"o}lich and M H{\"u}ll and J Wiltfang and M Scherer and S Riedel‐Heller and A Schneider and MT Heneka and K Fliessbach and A Sharaf and H Thiele and M Lennarz and F Jessen and W Maier and C Kubisch and Z Ignatova and P N{\"u}rnberg and P Pastor and J Walter and A Ramirez",

year = "2019",

month = aug,

day = "25",

doi = "10.1002/humu.23904",

language = "English",

volume = "0",

journal = "Human Mutation",

issn = "1059-7794",

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Karsak, M, Glebov, K, Scheffold, M, Bajaj, T, Kawalia, A, Karaca, I, Rading, S, Kornhuber, J, Peters, O, Diez‐Fairen, M, Frölich, L, Hüll, M, Wiltfang, J, Scherer, M, Riedel‐Heller, S, Schneider, A, Heneka, MT, Fliessbach, K, Sharaf, A, Thiele, H, Lennarz, M, Jessen, F, Maier, W, Kubisch, C, Ignatova, Z, Nürnberg, P, Pastor, P, Walter, J & Ramirez, A 2019, 'A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2', Human Mutation, vol. 0, no. 0. https://doi.org/10.1002/humu.23904

TY - JOUR

T1 - A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

AU - Karsak, M

AU - Glebov, K

AU - Scheffold, M

AU - Bajaj, T

AU - Kawalia, A

AU - Karaca, I

AU - Rading, S

AU - Kornhuber, J

AU - Peters, O

AU - Diez‐Fairen, M

AU - Frölich, L

AU - Hüll, M

AU - Wiltfang, J

AU - Scherer, M

AU - Riedel‐Heller, S

AU - Schneider, A

AU - Heneka, MT

AU - Fliessbach, K

AU - Sharaf, A

AU - Thiele, H

AU - Lennarz, M

AU - Jessen, F

AU - Maier, W

AU - Kubisch, C

AU - Ignatova, Z

AU - Nürnberg, P

AU - Pastor, P

AU - Walter, J

AU - Ramirez, A

PY - 2019/8/25

Y1 - 2019/8/25

UR - https://pearl.plymouth.ac.uk/pms-research/719/

U2 - 10.1002/humu.23904

DO - 10.1002/humu.23904

M3 - Article

SN - 1059-7794

VL - 0

JO - Human Mutation

JF - Human Mutation

IS - 0

ER -

A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2

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