(PDF) Erratum To: Segregation of S292F TPO Gene Mutation in

Erratum To: Segregation of S292F TPO Gene Mutation in Three Large Tunisian Families With Thyroid Dyshormonogenesis: Evidence of a Founder Effect

European Journal of Pediatrics - Germany

doi 10.1007/s00431-015-2669-3

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Date

November 14, 2015

Authors

Noura Bougacha-Elleuch

Publisher

Springer Science and Business Media LLC

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Erratum To: Segregation of S292F TPO Gene Mutation in Three Large Tunisian Families With Thyroid Dyshormonogenesis: Evidence of a Founder Effect

European Journal of Pediatrics - Germany

doi 10.1007/s00431-015-2669-3

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Phenotype of Three Consanguineous Tunisian Families With Early-Onset Retinal Degeneration Caused by an R91W Homozygous Mutation in the RPE65 Gene

Prevalence of C.2268dup and Detection of Two Novel Alterations, C.670_672del and C.1186C>T, in the TPO Gene in a Cohort of Malaysian-Chinese With Thyroid Dyshormonogenesis

Phenotypic Heterogeneity in British Patients With a Founder Mutation in the FHL1 Gene

The 752delG26 Mutation in the RFXANK Gene Associated With Major Histocompatibility Complex Class II Deficiency: Evidence for a Founder Effect in the Moroccan Population

Growth Hormone Insensitivity With Immune Dysfunction Caused by a STAT5B Mutation in the South of Brazil: Evidence for a Founder Effect

Founder Mutation(s) in theRSPH9Gene Leading to Primary Ciliary Dyskinesia in Two Inbred Bedouin Families

Novel Splice Site IDUA Gene Mutation in Tunisian Pedigrees With Hurler Syndrome

High Prevalence of a Missense Mutation of the Glucokinase Gene in Gestational Diabetic Patients Due to a Founder-Effect in a Local Population

Screening of Nineteen Unrelated Families With Generalized Resistance to Thyroid Hormone for Known Point Mutations in the Thyroid Hormone Receptor Beta Gene and the Detection of a New Mutation.