48,830
edits
Difference between revisions of "Cowden syndrome"
Jump to navigation
Jump to search
→Molecular: more
(→Molecular: more) |
|||
| 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> | ||