Researchclopedia
Research
Researchers
Institutions
Topics
Submit
About
Search...
⌘
K
Command Palette
Search for a command to run...
Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy | Researchclopedia
Back to research
Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy
2002
225 citations
Journal Article
Field-Weighted Citation Impact:
8.50
·
University of Helsinki
Carina Wallgren‐Pettersson
·
University of Helsinki