Cite
HARVARD Citation
Chilton, I. et al. (2020). De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype. American journal of medical genetics. 182 (5), pp. 962-973. [Online].
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Chilton, I. et al. (2020). De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype. American journal of medical genetics. 182 (5), pp. 962-973. [Online].