Your browser doesn't support javascript.
loading
A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy.
Miao, Jing; Wei, Xiao-Jing; Wang, Xu; Yin, Xiang; Yu, Xue-Fan.
Affiliation
  • Miao J; Department of Neurology and Neuroscience Center, the First Affiliated Hospital of Jilin University, Changchun, Jilin, People's Republic of China.
Medicine (Baltimore) ; 99(41): e22663, 2020 Oct 09.
Article in En | MEDLINE | ID: mdl-33031330
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multienzyme Complexes / Muscular Diseases Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Medicine (Baltimore) Year: 2020 Document type: Article Country of publication: Estados Unidos
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multienzyme Complexes / Muscular Diseases Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Medicine (Baltimore) Year: 2020 Document type: Article Country of publication: Estados Unidos