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Genomic newborn screening: BabyScreen+ v0.413 MYO9A Zornitza Stark Marked gene: MYO9A as ready
Genomic newborn screening: BabyScreen+ v0.413 MYO9A Zornitza Stark Gene: myo9a has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.413 MYO9A Zornitza Stark Classified gene: MYO9A as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.413 MYO9A Zornitza Stark Gene: myo9a has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.412 MYO9A Zornitza Stark reviewed gene: MYO9A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Myasthenic syndrome, congenital, 24, presynaptic (MIM# 618198); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.274 MYO9A David Amor reviewed gene: MYO9A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Myasthenic syndrome, congenital, 24, presynaptic; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 MYO9A Zornitza Stark gene: MYO9A was added
gene: MYO9A was added to gNBS. Sources: BeginNGS,Expert Review Green
Mode of inheritance for gene: MYO9A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYO9A were set to Myasthenic syndrome, congenital, 24, presynaptic, MIM# 618198