Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy"

Kishore R. Kumar; Christine Klein

doi:10.1002/mds.25089

Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy"

Kishore R. Kumar, Christine Klein^*

^*Corresponding author for this work

Institute of Neurogenetics

Royal North Shore Hospital

Original language	English
Journal	Movement Disorders
Volume	29
Issue number	7
Pages (from-to)	E1-E2
ISSN	0885-3185
DOIs	https://doi.org/10.1002/mds.25089
Publication status	Published - 06.2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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title = "Commentary for {"}Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy{"}",

author = "Kumar, \{Kishore R.\} and Christine Klein",

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T1 - Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy"

AU - Kumar, Kishore R.

AU - Klein, Christine

PY - 2014/6

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UR - https://www.scopus.com/pages/publications/84902279182

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M3 - Journal articles

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JO - Movement Disorders

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Commentary for "Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy"

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