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SREP41803
SREP41803
http://dx.doi.org/10.1038/SREP41803
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
P356
Q37644369-699C47A1-F163-426E-A965-C9C980685CDE
P356
SREP41803
http://dx.doi.org/10.1038/SREP41803