Fingerprint
Dive into the research topics of 'Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder
Nina B. Gold, Dong Li, Anna Chassevent, Frank J. Kaiser, Ilaria Parenti, Tim M. Strom, Feliciano J. Ramos, Beatriz Puisac, Juan Pié, Kirsty McWalter, Maria J. Guillen Sacoto, Hong Cui, Reem Saadeh-Haddad, Constance Smith-Hicks, Lance Rodan, Edward Blair, Elizabeth Bhoj
Research output: Contribution to journal › Article › peer-review