Autor: JMG Online First
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Correction 2: A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct
On the last 3 rows/lines (subjects 2106, 2107, 2108) of table 4 on page 670, the Allele 1 genotype «p.Asp324Tyr» should be «p.Asn324Tyr». This error does not change, in any way, the conclusions of the paper.
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Correction: SETD1B-associated neurodevelopmental disorder
Roston A, Evans D, Gill H et al, EPGEN Study. SETD1B-associated neurodevelopmental disorder. J Med Genet 2021;58:196–204. doi: 10.1136/jmedgenet-2019-106756There is a typographical error in Individual 3’s reported nucleotide sequence. Curre…