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Chatron, N. et al. (2017). A novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease. Clinical genetics. 92 (1), pp. 112-114. [Online].
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Chatron, N. et al. (2017). A novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease. Clinical genetics. 92 (1), pp. 112-114. [Online].