PUBMED ID | 22585553 |
DOI | 10.1002/ajmg.a.35363 |
TITLE | A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with aPTPN11mutation and a novel variant inSOS1 |
1 combination linked to 796 | OLI568 |
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PUBMED ID | 22585553 |
DOI | 10.1002/ajmg.a.35363 |
TITLE | A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with aPTPN11mutation and a novel variant inSOS1 |
1 combination linked to 796 | OLI568 |