Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.

Matthis Synofzik; Christoph Born; Axel Rominger; Nina Lummel; Ludger Schöls; Saskia Biskup; Cornelius Schüle; Ute Grasshoff; Thomas Klopstock; Christopher Adamczyk

doi:10.1016/j.neurobiolaging.2013.10.092

Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.

Matthis Synofzik, Christoph Born (Co-author), Axel Rominger, Nina Lummel, Ludger Schöls, Saskia Biskup, Cornelius Schüle, Ute Grasshoff, Thomas Klopstock, Christopher Adamczyk

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

38 Citations (Web of Science)

Original language	English
Pages (from-to)	1212.e1-1212.e5
Journal	NEUROBIOLOGY OF AGING
Volume	35
Issue number	5
DOIs	https://doi.org/10.1016/j.neurobiolaging.2013.10.092
Publication status	Published - 2014

Keywords

AMYOTROPHIC-LATERAL-SCLEROSIS
FRONTOTEMPORAL LOBAR DEGENERATION
BEHAVIORAL VARIANT
DEMENTIA
GENE
TDP-43

Access to Document

10.1016/j.neurobiolaging.2013.10.092

Cite this

Synofzik, M., Born, C., Rominger, A., Lummel, N., Schöls, L., Biskup, S., Schüle, C., Grasshoff, U., Klopstock, T., & Adamczyk, C. (2014). Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. NEUROBIOLOGY OF AGING , 35(5), 1212.e1-1212.e5. https://doi.org/10.1016/j.neurobiolaging.2013.10.092

Synofzik, Matthis ; Born, Christoph ; Rominger, Axel et al. / Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. In: NEUROBIOLOGY OF AGING 2014 ; Vol. 35, No. 5. pp. 1212.e1-1212.e5.

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title = "Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.",

keywords = "AMYOTROPHIC-LATERAL-SCLEROSIS, FRONTOTEMPORAL LOBAR DEGENERATION, BEHAVIORAL VARIANT, DEMENTIA, GENE, TDP-43",

author = "Matthis Synofzik and Christoph Born and Axel Rominger and Nina Lummel and Ludger Sch{\"o}ls and Saskia Biskup and Cornelius Sch{\"u}le and Ute Grasshoff and Thomas Klopstock and Christopher Adamczyk",

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doi = "10.1016/j.neurobiolaging.2013.10.092",

language = "English",

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Synofzik, M, Born, C, Rominger, A, Lummel, N, Schöls, L, Biskup, S, Schüle, C, Grasshoff, U, Klopstock, T & Adamczyk, C 2014, 'Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.', NEUROBIOLOGY OF AGING , vol. 35, no. 5, pp. 1212.e1-1212.e5. https://doi.org/10.1016/j.neurobiolaging.2013.10.092

Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. / Synofzik, Matthis; Born, Christoph (Co-author); Rominger, Axel et al.
In: NEUROBIOLOGY OF AGING , Vol. 35, No. 5, 2014, p. 1212.e1-1212.e5.

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

TY - JOUR

T1 - Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.

AU - Synofzik, Matthis

AU - Born, Christoph

AU - Rominger, Axel

AU - Lummel, Nina

AU - Schöls, Ludger

AU - Biskup, Saskia

AU - Schüle, Cornelius

AU - Grasshoff, Ute

AU - Klopstock, Thomas

AU - Adamczyk, Christopher

PY - 2014

Y1 - 2014

KW - AMYOTROPHIC-LATERAL-SCLEROSIS

KW - FRONTOTEMPORAL LOBAR DEGENERATION

KW - BEHAVIORAL VARIANT

KW - DEMENTIA

KW - GENE

KW - TDP-43

U2 - 10.1016/j.neurobiolaging.2013.10.092

DO - 10.1016/j.neurobiolaging.2013.10.092

M3 - Original Article

C2 - 24300238

SN - 0197-4580

VL - 35

SP - 1212.e1-1212.e5

JO - NEUROBIOLOGY OF AGING

JF - NEUROBIOLOGY OF AGING

IS - 5

ER -

Synofzik M, Born C, Rominger A, Lummel N, Schöls L, Biskup S et al. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. NEUROBIOLOGY OF AGING . 2014;35(5):1212.e1-1212.e5. doi: 10.1016/j.neurobiolaging.2013.10.092