Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype
- 1 July 2006
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 79 (1), 129-135
- https://doi.org/10.1086/504394
Abstract
No abstract availableKeywords
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