A novel homozygous truncating mutation of the SFRP4 gene in Pyle's disease. Issue 1 (16th January 2017)

• Record Type: Journal Article
• Authors: Chatron, N.; Lesca, G.; Labalme, A.; Rollat‐Farnier, P.A.; Monin, P.; Pichot, E.; Edery, P.; Sanlaville, D.; Rossi, M.
• Is Part Of: Clinical genetics. Volume 92:Issue 1(2017)
• Page Start: 112
• Page End: 114
• Publication Date: 2017-01-16
• Subjects: Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.12907
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :