A mouse model of brittle cornea syndrome caused by mutation in Zfp469
Brittle cornea syndrome (BCS) is a rare recessive condition characterised by extreme thinning of the cornea and sclera. BCS results from loss-of-function mutations in the poorly understood genes ZNF469 or PRDM5. In order to determine the function of ZNF469 and to elucidate pathogenic mechanisms, we...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2021-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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