RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort.

(2013) Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families.. This is an open-access article distributed under the terms of the Creative

(2015) Correction: Association between Childhood Strabismus and Refractive Error in Chinese Preschool Children.. This is an open access article distributed under the terms of

(2008) A Novel Gene, fudoh, in the SCCmec Region Suppresses the Colony Spreading Ability and Virulence of Staphylococcus aureus.. This is an open-access article distributed under

(2016) Attention Deficit/ Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children.. This is an open access article distributed under the

Three novel missense mutations were found in the MYH6 gene encoding alpha-myosin heavy chain ( R17H , C539R , and K543R ).. These mutations co-segregated with CHD in the families

(2014) Whole-Exome Sequencing Identifies a Novel Genotype-Phenotype Correlation in the Entactin Domain of the Known Deafness Gene TECTA.. This is an open-access article

(2014) Exome Sequencing Is an Efficient Tool for Variant Late-Infantile Neuronal Ceroid Lipofuscinosis Molecular Diagnosis.. This is an open-access article distributed under the

(2015) Adherence to Disease Modifying Drugs among Patients with Multiple Sclerosis in Germany: A Retrospective Cohort Study.. This is an open access article distributed under the