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S10038-017-0383-X
S10038-017-0383-X
http://dx.doi.org/10.1038/S10038-017-0383-X
Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathy.
P356
Q47372155-BAAC09E3-2B44-4C1A-9AF3-2D7EB79A8731
P356
S10038-017-0383-X
http://dx.doi.org/10.1038/S10038-017-0383-X