Home > Publications Database > A report of whole-genome sequencing in neurologic Wilson's disease. > print

001     139267
005     20240321220604.0
024 7 _ |a 10.4103/neuroindia.NI_1274_16
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024 7 _ |a 0028-3886
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024 7 _ |a 1998-4022
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024 7 _ |a altmetric:20046058
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037 _ _ |a DZNE-2020-05589
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Anwarullah, Anwarullah
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245 _ _ |a A report of whole-genome sequencing in neurologic Wilson's disease.
260 _ _ |a Chandigarh
|c 2017
|b Soc.
264 _ 1 |3 print
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|c 2017-01-01
336 7 _ |a article
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336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a Journal Article
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536 _ _ |a 341 - Molecular Signaling (POF3-341)
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650 _ 7 |a ATP7B protein, human
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650 _ 7 |a Copper-Transporting ATPases
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650 _ 2 |a Copper-Transporting ATPases: genetics
|2 MeSH
650 _ 2 |a DNA Mutational Analysis: methods
|2 MeSH
650 _ 2 |a Hepatolenticular Degeneration: complications
|2 MeSH
650 _ 2 |a Hepatolenticular Degeneration: genetics
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Mutation: genetics
|2 MeSH
650 _ 2 |a Nervous System Diseases: etiology
|2 MeSH
650 _ 2 |a Young Adult
|2 MeSH
700 1 _ |a Paramasivam, Nagarajan
|b 1
700 1 _ |a Abbasi, Rashda
|b 2
700 1 _ |a Khan, Kafaitullah
|b 3
700 1 _ |a Sultan, Aneesa
|b 4
700 1 _ |a Schlesner, Matthias
|b 5
700 1 _ |a von Engelhardt, Jakob
|b 6
700 1 _ |a Ahmad, Nafees
|b 7
700 1 _ |a Aslam, Muhammad
|0 P:(DE-2719)2810579
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773 1 8 |a 10.4103/neuroindia.ni_1274_16
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|t Neurology India
|v 65
|y 2017
|x 0028-3886
773 _ _ |a 10.4103/neuroindia.NI_1274_16
|g Vol. 65, no. 3, p. 629 -
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
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|v Molecular Signaling
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914 1 _ |y 2017
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920 1 _ |0 I:(DE-2719)1013023
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980 _ _ |a UNRESTRICTED

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