WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts
© 2019, The Author(s) under exclusive licence to The Japan Society of Human Genetics. A rare form of osteogenesis imperfecta (OI) caused by Wingless-type MMTV integration site family 1 (WNT1) mutations combines central nervous system (CNS) anomalies with the characteristic increased susceptibility t...
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| Main Authors: | , , , , , , , , |
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| Format: | Journal |
| Published: |
2019
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| Subjects: | |
| Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060775236&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/63570 |
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| Institution: | Chiang Mai University |