Your browser doesn't support javascript.
loading
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegia.
Fu, Jing-Xin; Wei, Qiao; Chen, Yu-Lan; Li, Hong-Fu.
Affiliation
  • Fu JX; Department of Neurology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • Wei Q; Department of Neurology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • Chen YL; Department of Neurology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • Li HF; Department of Medical Genetics, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Clin Genet ; 103(1): 87-92, 2023 01.
Article in En | MEDLINE | ID: mdl-36046950
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spastic Paraplegia, Hereditary / Neurodegenerative Diseases / Ubiquitin-Protein Ligases Limits: Adolescent / Humans Language: En Journal: Clin Genet Year: 2023 Document type: Article Affiliation country: 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: Spastic Paraplegia, Hereditary / Neurodegenerative Diseases / Ubiquitin-Protein Ligases Limits: Adolescent / Humans Language: En Journal: Clin Genet Year: 2023 Document type: Article Affiliation country: Country of publication: