Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay
Crossref DOI link: https://doi.org/10.1007/s11011-014-9618-0
Published Online: 2014-09-17
Published Print: 2015-06
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Ben-Salem, Salma
Gleeson, Joseph G.
Al-Shamsi, Aisha M.
Islam, Barira
Hertecant, Jozef
Ali, Bassam R.
Al-Gazali, Lihadh
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