Whole-exome sequencing identifies two novel missense mutations (p.L111P and p.R3048C) of RYR3 in a Vietnamese patient with autism spectrum disorders
Crossref DOI link: https://doi.org/10.1007/s13258-016-0495-2
Published Online: 2016-11-16
Published Print: 2017-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Nguyen, Thu Hien
Nguyen, Thi Thanh Ngan
Le, Bac Viet
Thanh, Ngoc Minh
Nguyen, Thi Kim Lien
Nong, Van Hai
Nguyen, Huy Hoang
Funding for this research was provided by:
Vietnam Academy of Science and Technology (VAST02.02/15-16)
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