Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency

Publisher: John Wiley & Sons Inc

E-ISSN: 2050-0904|6|1|200-205

ISSN: 2050-0904

Source: Clinical Case Reports, Vol.6, Iss.1, 2018-01, pp. : 200-205

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract