Τρίτη 27 Νοεμβρίου 2018

A family with PTEN mutations with malignancy and an unusually high number of offspring with autism spectrum disorder: a case report

Cowden's syndrome (OMIM:158350), a rare genetic disorder (incidence ~ 1:250,000), is caused by mutations of the tumor suppressor gene PTEN. In this report, we describe clinical manifestations of a 56-year-old pat...

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