A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.

TitleA postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
Publication TypeJournal Article
AuthorsZieba, J, Zhang, W, Chong, JX, Forlenza, KN, Martin, JH, Heard, K, Grange, DK, Butler, MG, Kleefstra, T, Lachman, RS, Nickerson, D, Regnier, M, Cohn, DH, Bamshad, M, Krakow, D
PubMed ID28205584
PubMed Central IDPMC5311977
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
UL1 TR000124 / TR / NCATS NIH HHS / United States
F31 AR066487 / AR / NIAMS NIH HHS / United States
R01 AR066124 / AR / NIAMS NIH HHS / United States
R01 AR062651 / AR / NIAMS NIH HHS / United States