Bi‐allelic loss of function variants in <scp>GOLGA2</scp> are associated with a complex neurological phenotype: Report of a second family

Udhaya Kotecha(Center for Genomic Science), Vandana Gupta(Brigham and Women's Hospital), Nidhi Shah(Nassau University Medical Center), Mehul Mistri(Center for Genomic Science), Parth Shah(Dartmouth College)
Clinical Genetics
August 23, 2021
Cited by 8


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