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Ankyrins

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Resolving a Complex Neonatal Phenotype by Rapid Trio Whole-Genome Sequencing: A De Novo 11q14.3-q22.3 Deletion and a Splicing-Altering Synonymous ANK1 Variant.
Ankyrins
Lithium treatment drives coordinated multi-kinase remodelling of the mouse synaptic phosphoproteome
Ankyrins
Clinicohematological and Genetic Profile of Hereditary Spherocytosis in Children: An Experience From a North Indian Center.
Ankyrins
Discovery of a potential novel pharmacogenomic biomarker on ANK3 gene for liafensine, a triple reuptake inhibitor for treatment-resistant depression.
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Expanding the genetic spectrum of hereditary spherocytosis: novel mutations and phenotypic heterogeneity from a 55-patient cohort.
Ankyrins
In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis.
Ankyrins
Lithium drives coordinated changes in the mouse synaptic phosphoproteome
Ankyrins
A new case of hereditary spherocytosis with a gain-of-function SPTB mutation
Ankyrins
De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review.
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Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children.
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