Title: | A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies |
Journal : | Neuromuscular disorders : NMD, 23, 5 |
Authors: | D'Amico A ; Fattori F ; Bellacchio E ; Catteruccia M ; Servidei S ; Bertini E |
Material Type: | Article |
Publication Date: | 2013 |
Size: | p. 437-440 |
Languages: | English |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/23489661 |
Pubmed / DOI : | DOI : 10.1016/j.nmd.2013.02.011 |