1-3 of 3
Authors: Kimio Tomita
Journal Article
Mutations in Human Urate Transporter 1 Gene in Presecretory Reabsorption Defect Type of Familial Renal Hypouricemia Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 90, Issue 4, 1 April 2005, Pages 2169–2174, https://doi.org/10.1210/jc.2004-1111
Published: 01 April 2005
Journal Article
Liddle’s Syndrome Caused by a Novel Mutation in the Proline-Rich PY Motif of the Epithelial Sodium Channel β-Subunit Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 90, Issue 1, 1 January 2005, Pages 340–344, https://doi.org/10.1210/jc.2004-1027
Published: 01 January 2005
Journal Article
A Family with Liddle’s Syndrome Caused by a New Missense Mutation in the β Subunit of the Epithelial Sodium Channel Get access
The Journal of Clinical Endocrinology & Metabolism, Volume 83, Issue 6, 1 June 1998, Pages 2210–2213, https://doi.org/10.1210/jcem.83.6.5030
Published: 01 June 1998
