Variant nomenclature discrepancy was identified in the article “Expanding the genetic heterogeneity of intellectual disability”, Human Genetics, November 2017, Volume 136, Issue 11-12, pp 1419-1429 after its publication. Specifically, the nomenclature of GTF3C3 was originally listed as NM_012086.4:c.1382+3A>G when it should be NM_012086.4:c.1390+3A>G, the nomenclature of MADD was originally listed as NM_001135943.1:c.2930T>G:p.(Val977Gly) when it should be NM_001135943.1:c.2930T>G:p.(Leu977Arg), and the variant NM_001164416.1:c.124C>T:p.(Arg42*) was listed under the gene's name VWA3B when it should be H2BFM. The following changes were made in the attached corrections: 1. Nomenclature of GTF3C3 is changed to NM_012086.4:c.1390+3A>G in 15DG0315 (from NM_012086.4:c.1382+3A>G) in the main text, Table S1, Table S2 and Figure S1. 2. The variant NM_001164416.1:c.124C>T:p.(Arg42*) in 17DG0782 is now correctly listed under the name H2BFM in the abstract, Table 1, Table S1 and Table S2. 3. Nomenclature of MADD is changed to NM_001135943.1:c.2930T>G:p.(Leu977Arg) in 17DG0771 (From NM_001135943.1:c.2930T>G:p. (Val977Gly) in results, Table 1, Table S1, and Table S2. The authors sincerely apologize for these errors and appreciate the opportunity to mend the records.
File in questo prodotto:
Non ci sono file associati a questo prodotto.