LE WE PMID CA
ATP7A9408ATP7A

ATP7A

ATP7B

BSCL2 Seipin

Cisplatin

Copper

Ctr1

CTR2

DCTN1

DYNC1H1

GARS

HSPB1

HSPB3

HspB8

IGHMBP2

Menkes s disease

Nervous system (Inherited diseases)

PLEKHG5

SETX

Transporter (Copper)

TRPV4

Wilson s disease

2010  
1
Mammalian copper-transporting P-type ATPases, ATP7A and ATP7B: emerging roles.
[19922814] Int J Biochem Cell Biol 42(2): 206-9 (2010)
2007  
2
Biochemical basis of regulation of human copper-transporting ATPases.
[17562324] Arch Biochem Biophys 463(2): 134-48 (2007)
2010  
3
2011  
4
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  
5
The distal hereditary motor neuropathies.
[22028385] J Neurol Neurosurg Psychiatry 83(1): 6-14 (2012)
2009  
6
Human copper transporters: mechanism, role in human diseases and therapeutic potential.
[20454597] Future Med Chem 1(6): 1125-42 (2009)
2007  
7
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
[17717039] J Med Genet 44(11): 673-88 (2007)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.



  • ATP7A

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