Cite
HARVARD Citation
Böhm, J. et al. (2019). Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures. Journal of medical genetics. 56 (9), pp. 617-621. [Online].
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Böhm, J. et al. (2019). Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures. Journal of medical genetics. 56 (9), pp. 617-621. [Online].