TGFBR2

Syndromic aortopathy — overlap with Loeys–Dietz syndrome 2 (MIM#610168)

1 article(s) in the watch · Constitutional genetics

Curated publications

Rare missense variants in TGFBR2 and FLNA identified by whole-exome sequencing in syndromic genetic aortopathy

Syndromic aortopathy — overlap with Loeys–Dietz syndrome 2 (MIM#610168)

Automatic aggregation page — a clinical introduction may be added.