Cite
HARVARD Citation
Meier, N. et al. (2017). A novel homozygous splice‐site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle development. Prenatal diagnosis. pp. 720-724. [Online].
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Meier, N. et al. (2017). A novel homozygous splice‐site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle development. Prenatal diagnosis. pp. 720-724. [Online].