A Novel Mutation in the β-Subunit of the Epithelial Sodium Channel Gene (SCNNIB) in a Thai Family with Liddle's Syndrome

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. Current Developments in Wolfram Syndrome
4. Transient Neonatal Hypothyroidism Manifested at Birth
5. Secular Trend in Body Height of Schoolchildren in Northeast Attica, Greece
6. High and Low Birth Weight and its Implication for Growth and Bone Development in Childhood and Adolescence
7. Auxological Evaluation and Determinants of Growth Failure at the Time of Adoption in Eastern European Adoptees
8. Difference Between Japanese and Caucasian Populations in the Allelic Frequency of Growth Hormone Receptor Polymorphisms
9. Facial Metrics in Children with Corticotrophin-Producing Pituitary Adenomas Suggest Abnormalities in Midface Development
10. Safety and Efficacy of Intravenous Zoledronic Acid in Paediatric Osteoporosis
11. Pediatric Atorvastatin in Diabetes Trial (PADIT): A Pilot Study to Determine the Effect of Atorvastatin on Arterial Stiffness and Endothelial Function in Children with Type 1 Diabetes Mellitus
12. Phthalate Exposure in Girls During Early Puberty
13. Feminizing Adrenocortical Adenoma in a 5 Year-old Girl
14. A Novel Mutation in the β-Subunit of the Epithelial Sodium Channel Gene (SCNNIB) in a Thai Family with Liddle's Syndrome
15. A Novel Nonsense Mutation of the Mineralocorticoid Receptor Gene in the Renal Form of Pseudohypoaldosteronism Type 1
16. A Healthy, Female Chimera with 46,XX/46,XY Karyotype
17. CALENDAR
18. List of Reviewers for 2008