(Q44760138)

6 December 2017

title

Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia (English)

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6 December 2017

Melanie Hamann

1

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6 December 2017

Miriam H Meisler

series ordinal

2

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6 December 2017

Angelika Richter

series ordinal

3

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6 December 2017

language of work or name

English

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publication date

1 December 2003

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6 December 2017

published in

Experimental Neurology

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6 December 2017

volume

184

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6 December 2017

issue

2

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6 December 2017

page(s)

830-838

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Dopamine transmission in DYT1 dystonia: a biochemical and autoradiographical study

6 December 2017

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7 January 2021

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The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons.

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Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis

7 January 2021

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7 January 2021

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7 January 2021

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Mutational and biochemical analysis of dopamine in dystonia: evidence for decreased dopamine D2 receptor inhibition

7 January 2021

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Stereological methods for estimating the total number of neurons and synapses: issues of precision and bias

7 January 2021

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10.1016/S0014-4886(03)00290-5

7 January 2021

Identifiers

DOI

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6 December 2017

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