000139267 001__ 139267
000139267 005__ 20240321220604.0
000139267 0247_ $$2doi$$a10.4103/neuroindia.NI_1274_16
000139267 0247_ $$2pmid$$apmid:28488633
000139267 0247_ $$2ISSN$$a0028-3886
000139267 0247_ $$2ISSN$$a1998-4022
000139267 0247_ $$2altmetric$$aaltmetric:20046058
000139267 037__ $$aDZNE-2020-05589
000139267 041__ $$aEnglish
000139267 082__ $$a610
000139267 1001_ $$0P:(DE-2719)9000009$$aAnwarullah, Anwarullah$$b0$$eFirst author$$udzne
000139267 245__ $$aA report of whole-genome sequencing in neurologic Wilson's disease.
000139267 260__ $$aChandigarh$$bSoc.$$c2017
000139267 264_1 $$2Crossref$$3print$$bMedknow$$c2017-01-01
000139267 3367_ $$2DRIVER$$aarticle
000139267 3367_ $$2DataCite$$aOutput Types/Journal article
000139267 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1590755848_15073$$xLetter
000139267 3367_ $$2BibTeX$$aARTICLE
000139267 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000139267 3367_ $$00$$2EndNote$$aJournal Article
000139267 536__ $$0G:(DE-HGF)POF3-341$$a341 - Molecular Signaling (POF3-341)$$cPOF3-341$$fPOF III$$x0
000139267 588__ $$aDataset connected to CrossRef, PubMed,
000139267 650_7 $$0EC 7.2.2.8$$2NLM Chemicals$$aATP7B protein, human
000139267 650_7 $$0EC 7.2.2.8$$2NLM Chemicals$$aCopper-Transporting ATPases
000139267 650_2 $$2MeSH$$aCopper-Transporting ATPases: genetics
000139267 650_2 $$2MeSH$$aDNA Mutational Analysis: methods
000139267 650_2 $$2MeSH$$aHepatolenticular Degeneration: complications
000139267 650_2 $$2MeSH$$aHepatolenticular Degeneration: genetics
000139267 650_2 $$2MeSH$$aHumans
000139267 650_2 $$2MeSH$$aMale
000139267 650_2 $$2MeSH$$aMutation: genetics
000139267 650_2 $$2MeSH$$aNervous System Diseases: etiology
000139267 650_2 $$2MeSH$$aYoung Adult
000139267 7001_ $$aParamasivam, Nagarajan$$b1
000139267 7001_ $$aAbbasi, Rashda$$b2
000139267 7001_ $$aKhan, Kafaitullah$$b3
000139267 7001_ $$aSultan, Aneesa$$b4
000139267 7001_ $$aSchlesner, Matthias$$b5
000139267 7001_ $$avon Engelhardt, Jakob$$b6
000139267 7001_ $$aAhmad, Nafees$$b7
000139267 7001_ $$0P:(DE-2719)2810579$$aAslam, Muhammad$$b8$$eLast author$$udzne
000139267 77318 $$2Crossref$$3journal-article$$a10.4103/neuroindia.ni_1274_16$$b : Medknow, 2017-01-01$$n3$$p629$$tNeurology India$$v65$$x0028-3886$$y2017
000139267 773__ $$0PERI:(DE-600)2058812-4$$a10.4103/neuroindia.NI_1274_16$$gVol. 65, no. 3, p. 629 -$$n3$$p629$$q65:3<629 -$$tNeurology India$$v65$$x0028-3886$$y2017
000139267 909CO $$ooai:pub.dzne.de:139267$$pVDB
000139267 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)9000009$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b0$$kDZNE
000139267 9101_ $$0I:(DE-588)1065079516$$6P:(DE-2719)2810579$$aDeutsches Zentrum für Neurodegenerative Erkrankungen$$b8$$kDZNE
000139267 9131_ $$0G:(DE-HGF)POF3-341$$1G:(DE-HGF)POF3-340$$2G:(DE-HGF)POF3-300$$aDE-HGF$$bForschungsbereich Gesundheit$$lErkrankungen des Nervensystems$$vMolecular Signaling$$x0
000139267 9141_ $$y2017
000139267 915__ $$0StatID:(DE-HGF)0200$$2StatID$$aDBCoverage$$bSCOPUS$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0300$$2StatID$$aDBCoverage$$bMedline$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0199$$2StatID$$aDBCoverage$$bClarivate Analytics Master Journal List$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0150$$2StatID$$aDBCoverage$$bWeb of Science Core Collection$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0100$$2StatID$$aJCR$$bNEUROL INDIA : 2021$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0600$$2StatID$$aDBCoverage$$bEbsco Academic Search$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)0030$$2StatID$$aPeer Review$$bASC$$d2022-11-12
000139267 915__ $$0StatID:(DE-HGF)9900$$2StatID$$aIF < 5$$d2022-11-12
000139267 9201_ $$0I:(DE-2719)1013023$$kAG Engelhardt$$lSynaptic Signalling and Neurodegeneration$$x0
000139267 980__ $$ajournal
000139267 980__ $$aVDB
000139267 980__ $$aI:(DE-2719)1013023
000139267 980__ $$aUNRESTRICTED