Pages that link to "Q50701250"

The following pages link to Muhammad Ansar (Q50701250):

Displaying 18 items.

• NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1b (Q21245104) (← links)
• Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders. (Q34326689) (← links)
• Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree (Q37099823) (← links)
• RNAi as a new therapeutic strategy against HCV. (Q37591580) (← links)
• Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay. (Q41918634) (← links)
• Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan. (Q42331832) (← links)
• Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. (Q42619208) (← links)
• Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice (Q50701179) (← links)
• Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3 (Q56636922) (← links)
• Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts (Q57023910) (← links)
• Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature (Q90026441) (← links)
• Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature (Q90677321) (← links)
• Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability (Q91254478) (← links)
• Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features (Q91957851) (← links)
• Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiency (Q92426727) (← links)
• Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature (Q93340232) (← links)
• New variants and in silico analyses in GRK1 associated Oguchi disease (Q103737028) (← links)
• A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome (Q124072752) (← links)