Article
SPECC1L-deficient palate mesenchyme cells show speed and directionality defect
2019-11-25
Abstract excerpt
Clefts of the lip and/or palate (CL/P) are common anomalies that occur in 1/800 live births. Pathogenic SPECC1L variants identified in patients with rare atypical clefts and syndromic CL/P suggest the gene plays a primary role in face and palate development. We have generated Specc1l gene-trap ( Specc1l cGT ) and truncation ( Specc1l ΔC510 ) alleles that cause embryonic or perinatal lethality, respectively....
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Identifiers and source
- Literature Corpus work
- e8efdd29-f23f-59aa-85aa-77192278cca2
- DOI
- 10.1101/854273
