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Intellectual disability - microarray and sequencing v2.955 SLC9A6 Rebecca Foulger Publications for gene: SLC9A6 were set to
Intellectual disability - microarray and sequencing v2.954 SLC9A6 Rebecca Foulger changed review comment from: Comment on mode of inheritance: Changed the MOI from XLR to XLD based on Pescosolido et al., 2014 (PMID:25044251) who report mild to moderate ID in heterozygous female carriers.; to: Comment on mode of inheritance: Changed the MOI from XLR to XLD based on Pescosolido et al., 2014 (PMID:25044251) who report mild to moderate ID in heterozygous female carriers. Note that NHE6 is an alias for SLC9A6.
Intellectual disability - microarray and sequencing v2.954 SLC9A6 Rebecca Foulger Added comment: Comment on mode of inheritance: Changed the MOI from XLR to XLD based on Pescosolido et al., 2014 (PMID:25044251) who report mild to moderate ID in heterozygous female carriers.
Intellectual disability - microarray and sequencing v2.954 SLC9A6 Rebecca Foulger Mode of inheritance for gene: SLC9A6 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Intellectual disability - microarray and sequencing v2.468 SLC9A6 Louise Daugherty Source Victorian Clinical Genetics Services was added to SLC9A6.
Intellectual disability - microarray and sequencing SLC9A6 BRIDGE consortium edited their review of SLC9A6
Intellectual disability - microarray and sequencing SLC9A6 BRIDGE consortium edited their review of SLC9A6
Intellectual disability - microarray and sequencing SLC9A6 BRIDGE consortium reviewed SLC9A6