Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis

New Research: Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis: Asparagine synthetase deficiency (ASNSD) is a rare congenital disorder characterized by… https://t.co/