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

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

scientific article published on 16 February 2017

Author/s

author: Jessica X. Chong, Ralph S. Lachman, Deborah A Nickerson, Dorothy K Grange, Tjitske Kleefstra

Work details

Publication date

February 16, 2017

Language

English

Copyright status

copyrighted