Your browser doesn't support javascript.
loading
Update on the Genetics of Congenital Myopathies.
Pelin, Katarina; Wallgren-Pettersson, Carina.
Affiliation
  • Pelin K; Molecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland; The Folkhälsan Institute of Genetics, Folkhälsan Research Center, and Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland. Electronic address: Katarina.Pelin@helsinki.fi.
  • Wallgren-Pettersson C; The Folkhälsan Institute of Genetics, Folkhälsan Research Center, and Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
Semin Pediatr Neurol ; 29: 12-22, 2019 04.
Article in En | MEDLINE | ID: mdl-31060721
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myopathies, Structural, Congenital / Genotype / Mutation Limits: Humans Language: En Journal: Semin Pediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2019 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: Myopathies, Structural, Congenital / Genotype / Mutation Limits: Humans Language: En Journal: Semin Pediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2019 Document type: Article Country of publication: