A Novel Genotype and Pathological Phenotype in a Patient with Myosin Heavy Chain 2A Myopathy (P5.440)
Year: 2018
Type: article
Study design: Case Report
Source: Neurology
Institutions: Mayo Clinic, UnityPoint Health
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W3186502668
