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Nervous system (Inherited diseases)
LE WE PMID CA
Nervous system (Inherited diseases)8720Nervensystem (Hereditaere Erkrankungen)

ATP7A

BSCL2 Seipin

DCTN1

DYNC1H1

GARS

HSPB1

HSPB3

HspB8

IGHMBP2

Ion channel (BASKET)

Ion channel (Sodium)

Mitochondria (BASKET)

Musculoskeletal system (Genetic diseases)

Nav1 7

Nervous system (Inherited diseases)

P2X7

Pain (Neurophysiology)

PLEKHG5

SETX

TRPV1

TRPV4

2010  
1
Neurological channelopathies: new insights into disease mechanisms and ion channel function.
[20375141] J Physiol 588(Pt 11): 1823-7 (2010)
2010  
2
Voltage-sensor mutations in channelopathies of skeletal muscle.
[20156847] J Physiol 588(Pt 11): 1887-95 (2010)
2010  
3
1999  
4
Genetic malformations of the human cerebral cortex.
[10402190] Neuron 23(1): 19-29 (1999)
2006  
5
The role of mitochondria in inherited neurodegenerative diseases.
[16805775] J Neurochem 97(6): 1659-75 (2006)
2011  
6
Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studies.
[21902652] Curr Mol Med 11(8): 650-65 (2011)
2012  
7
TRPV4 axonal neuropathy spectrum disorder.
[22617546] J Clin Neurosci 19(7): 927-33 (2012)
2010  
8
TRPV4-pathy, a novel channelopathy affecting diverse systems.
[20505684] J Hum Genet 55(7): 400-2 (2010)
2012  
9
The distal hereditary motor neuropathies.
[22028385] J Neurol Neurosurg Psychiatry 83(1): 6-14 (2012)
2011  
10
TRPV4 neuropathies: calcium channel inhibition as a therapeutic target?
[21288983] Neurology 76(10): 856-7 (2011)

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