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Article

A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome

13 Aug 2015

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26279204
DOI: 10.1016/j.ajhg.2015.07.009

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A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen SyndromePMID 26279204Read ↗

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