3-M syndrome: a growth disorder associated with IGF2 silencing
3-M syndrome is an autosomal recessive disorder characterised by pre- and postnatal growth restriction, facial dysmorphism, normal intelligence and radiological features (slender long bones and tall vertebral bodies). It is known to be caused by mutations in the genes encoding Cullin 7, Obscurin lik...
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2013-11.
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| Subjects: | |
| Online Access: | Get fulltext |