Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Rossella Spataro; Maria Kousi; Sali M. K. Farhan; Jason R. Willer; Jay P. Ross; Patrick A. Dion; Guy A. Rouleau; Mark J. Daly; Benjamin M. Neale; Vincenzo La Bella; Nicholas Katsanis

doi:10.1186/s40246-019-0203-9

Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

Rossella Spataro, Maria Kousi, Sali M. K. Farhan, Jason R. Willer, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau, Mark J. Daly, Benjamin M. Neale, Vincenzo La Bella, Nicholas Katsanis

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

Original language	English
Article number	19
Journal	Human Genomics
Volume	13
Number of pages	10
ISSN	1473-9542
DOIs	https://doi.org/10.1186/s40246-019-0203-9
Publication status	Published - 16 Apr 2019
MoE publication type	A1 Journal article-refereed

Fields of Science

PARKINSONISM
DEMENTIA
1184 Genetics, developmental biology, physiology

Access to Document

10.1186/s40246-019-0203-9

s40246-019-0203-9Final published version, 1.81 MBLicence: CC BY

Cite this

Spataro, R., Kousi, M., Farhan, S. M. K., Willer, J. R., Ross, J. P., Dion, P. A., Rouleau, G. A., Daly, M. J., Neale, B. M., La Bella, V., & Katsanis, N. (2019). Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion. Human Genomics, 13, [19]. https://doi.org/10.1186/s40246-019-0203-9

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title = "Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion",

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author = "Rossella Spataro and Maria Kousi and Farhan, {Sali M. K.} and Willer, {Jason R.} and Ross, {Jay P.} and Dion, {Patrick A.} and Rouleau, {Guy A.} and Daly, {Mark J.} and Neale, {Benjamin M.} and {La Bella}, Vincenzo and Nicholas Katsanis",

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T1 - Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion

AU - Spataro, Rossella

AU - Kousi, Maria

AU - Farhan, Sali M. K.

AU - Willer, Jason R.

AU - Ross, Jay P.

AU - Dion, Patrick A.

AU - Rouleau, Guy A.

AU - Daly, Mark J.

AU - Neale, Benjamin M.

AU - La Bella, Vincenzo

AU - Katsanis, Nicholas

PY - 2019/4/16

Y1 - 2019/4/16

KW - PARKINSONISM

KW - DEMENTIA

KW - 1184 Genetics, developmental biology, physiology

U2 - 10.1186/s40246-019-0203-9

DO - 10.1186/s40246-019-0203-9

M3 - Article

VL - 13

JO - Human Genomics

JF - Human Genomics

SN - 1473-9542

M1 - 19

ER -