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APA Citation
Chatron, N., Lesca, G., Labalme, A., Rollat‐Farnier, P., Monin, P., Pichot, E., Edery, P., Sanlaville, D., & Rossi, M. (2017). a novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease. Clinical genetics, 92(1), 112–114. http://access.bl.uk/ark:/81055/vdc_100047473505.0x00005c