Wikidata

(Q86454632)

English

A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy

scientific article published on 25 March 2013

In more languages

Statements

title
A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
23521069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23521069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 February 2020

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