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–Hitchcock Medical Center)
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