Found: 5
Select item for more details and to access through your institution.
A novel homozygous ALPK3 variant associated with cardiomyopathy and skeletal muscle involvement.
- Published in:
- Muscle & Nerve, 2022, v. 65, n. 3, p. E7, doi. 10.1002/mus.27471
- By:
- Publication type:
- Article
Phenotypic variability and molecular genetics in proximal myotonic myopathy.
- Published in:
- Muscle & Nerve, 2015, v. 51, n. 5, p. 686, doi. 10.1002/mus.24440
- By:
- Publication type:
- Article
Association of VEGF Gene Polymorphisms with the Development of Heart Failure in Patients after Myocardial Infarction.
- Published in:
- Cardiology, 2009, v. 114, n. 1, p. 11, doi. 10.1159/000210189
- By:
- Publication type:
- Article
Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 2, p. 179, doi. 10.1038/sj.ejhg.5200253
- By:
- Publication type:
- Article
3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype.
- Published in:
- Human Mutation, 1998, v. 11, p. S209, doi. 10.1002/humu.1380110168
- By:
- Publication type:
- Article