Journal Article (Letter)

DZNE-2020-05589

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png A report of whole-genome sequencing in neurologic Wilson's disease.

Anwarullah, A. (First author)DZNE* ; Paramasivam, N. ; Abbasi, R. ; Khan, K. ; Sultan, A. ; Schlesner, M. ; von Engelhardt, J. ; Ahmad, N. ; Aslam, M. (Last author)DZNE*

2017
Soc. Chandigarh

This record in other databases:    

Please use a persistent id in citations: doi:10.4103/neuroindia.NI_1274_16

Keyword(s): Copper-Transporting ATPases: genetics (MeSH) ; DNA Mutational Analysis: methods (MeSH) ; Hepatolenticular Degeneration: complications (MeSH) ; Hepatolenticular Degeneration: genetics (MeSH) ; Humans (MeSH) ; Male (MeSH) ; Mutation: genetics (MeSH) ; Nervous System Diseases: etiology (MeSH) ; Young Adult (MeSH) ; ATP7B protein, human ; Copper-Transporting ATPases

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Contributing Institute(s):

1. Synaptic Signalling and Neurodegeneration (AG Engelhardt)

Research Program(s):

1. 341 - Molecular Signaling (POF3-341) (POF3-341)

Appears in the scientific report 2017

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Database coverage:
; Clarivate Analytics Master Journal List ; Ebsco Academic Search ; IF < 5 ; JCR ; SCOPUS ; Web of Science Core Collection

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