Fig. 2From: The most 5′ truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case reportReported mutations in WNT1 [3,4,5,6,7, 9, 11,12,13,14,15] (solid bars represent coding exons of WNT1)Back to article page