Publication | Open Access
Insights from genotype–phenotype correlations by novel SPEG mutations causing centronuclear myopathy
35
Citations
11
References
2017
Year
Genetic DisorderNovel Speg MutationsGeneticsGenotype–phenotype CorrelationsMedicinePathologyMolecular GeneticsDisease Gene IdentificationMolecular DiagnosticsCentronuclear Myopathy
| Year | Citations | |
|---|---|---|
Page 1
Page 1