Heterozygous de novo variants...

Clinical Genetics 2020 / 10

Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder

Gold, Nina B., Li, Dong, Chassevent, Anna, Kaiser, Frank J., Parenti, Ilaria, Strom, Tim M., Ramos, Feliciano J., Puisac, Beatriz, Pié, Juan, McWalter, Kirsty, Guillen Sacoto, Maria J., Cui, Hong, Sa
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Journal:
Clinical Genetics
DOI:
10.1111/cge.13851
Date:
October, 2020
File:
PDF, 1.13 MB
2020
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