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Keywords: 22q11.2 deletion syndrome
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Journal Articles
Journal: Development
Development (2020) 147 (3): dev185256.
Published: 3 February 2020
..., in a distribution established in the early embryo. We further show that biallelic expression of the CPM regulatory gene Tbx1 , haploinsufficient in 22q11.2 deletion syndrome patients, is required for the correct patterning of muscles with CPM-derived connective tissue. Our results suggest that CPM plays...
Includes: Supplementary data
Journal Articles