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  <title>Episode 558 - Anton Morkin</title>
  <description>One Dad’s Mission to Cure His Son’s Genetic Disease When Anton Morkin’s son was diagnosed with “idiopathic” pulmonary hypertension, he refused to accept “no known cause” as an answer. What followed was a crash course in genetics, the discovery of a rare mutation, and the formation of a worldwide coalition, TBX4Life.   Learn more about pulmonary hypertension trials at&amp;amp;nbsp;www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure:&amp;amp;nbsp;www.phaware.global/donate&amp;amp;nbsp;#phaware  Share your story: info@phaware.global  Like, Subscribe and Follow us:  www.phawarepodcast.com.&amp;amp;nbsp;@TBX4_Life </description>
  <author_name>I'm Aware That I'm Rare: the phaware® podcast</author_name>
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