Phenotypic Variability in a Family With Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of PKA Phosphorylation
JCRPE Journal of Clinical Research in Pediatric Endocrinology - Turkey
doi 10.4274/jcrpe.4488
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Date
December 14, 2017
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Galenos Yayinevi