Severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features are due to a homozygous QARS mutation
Crossref DOI link: https://doi.org/10.1007/s10048-017-0516-6
Published Online: 2017-06-15
Published Print: 2017-07
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Leshinsky-Silver, Esther
Ling, Jiqiang
Wu, Jiang
Vinkler, Chana
Yosovich, Keren
Bahar, Sarit
Yanoov-Sharav, Miri
Lerman-Sagie, Tally
Lev, Dorit
License valid from 2017-06-15