Your browser doesn't support javascript.
loading
Kearns-Sayre syndrome with rare imaging finding of SLC25A4 Mutation.
Zhao, Huan; Shi, Min; Yang, Fang; Yang, Xuhong.
Affiliation
  • Zhao H; From the Department of Neurology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, People's Republic of China.
  • Shi M; From the Department of Neurology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, People's Republic of China.
  • Yang F; From the Department of Neurology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, People's Republic of China.
  • Yang X; From the Department of Neurology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan Province, People's Republic of China.
Neurosciences (Riyadh) ; 27(2): 111-115, 2022 Apr.
Article in En | MEDLINE | ID: mdl-35477912
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kearns-Sayre Syndrome / Ophthalmoplegia, Chronic Progressive External Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Neurosciences (Riyadh) Journal subject: NEUROLOGIA Year: 2022 Document type: Article Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kearns-Sayre Syndrome / Ophthalmoplegia, Chronic Progressive External Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Neurosciences (Riyadh) Journal subject: NEUROLOGIA Year: 2022 Document type: Article Country of publication: