Difference between revisions of "Cowden syndrome"

Jump to navigation Jump to search
Line 2: Line 2:


==Molecular==
==Molecular==
*PTEN mutation.
*Phosphatase and tensin homolog (PTEN) mutation.<ref name=omim601728>{{OMIM|601728}}</ref>
*Autosomal dominant inheritance.<ref name=OMIM158350>{{OMIM|158350}}</ref>
*Autosomal dominant inheritance.<ref name=OMIM158350>{{OMIM|158350}}</ref>