Cite
HARVARD Citation
Reinstein, E. et al. (2018). Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Clinical genetics. 93 (1), pp. 160-163. [Online].
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Reinstein, E. et al. (2018). Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Clinical genetics. 93 (1), pp. 160-163. [Online].