Cite
HARVARD Citation
Alisch, F. et al. (2017). Familial Gordon syndrome associated with a PIEZO2 mutation. American journal of medical genetics. 173 (1), pp. 254-259. [Online].
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Alisch, F. et al. (2017). Familial Gordon syndrome associated with a PIEZO2 mutation. American journal of medical genetics. 173 (1), pp. 254-259. [Online].