- Tytuł:
- G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features
- Autorzy:
- Źródło:
- In Neuromuscular Disorders October 2014 24(9-10):843-844
Czasopismo naukowe