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Part 21: MEMBRANE TRANSPORT DISORDERS

190:

Familial Glucose-Galactose Malabsorption and Hereditary Renal Glycosuria, Ernest M. Wright / Martín G. Martín / Eric Turk [Abstract] [Full Text]
191:

Cystinuria, Manuel Palacín / Paul Goodyer / Virginia Nunes / Paolo Gasparini [Abstract] [Full Text]
192:

Lysinuric Protein Intolerance and Other Cationic Aminoacidurias, Olli Simell [Abstract] [Full Text]
193:

Hartnup Disorder, Harvey L. Levy [Abstract] [Full Text]
194:

Iminoglycinuria, Stefan Bröer / Russell W. Chesney [Abstract] [Full Text] Revised—November 2010
195:

Renal Tubular Acidosis, Thomas D. DuBose, Jr. / Robert J. Alpern [Abstract] [Full Text]
196:

The Renal Fanconi Syndrome, Michel Bergeron / André Gougoux / Josette Noël / Lucie Parent [Abstract] [Full Text]
197:

Mendelian Hypophosphatemias, Alberto Auricchio / Yves Sabbagh / Harriet S. Tenenhouse / Michael J. Econs [Abstract] [Full Text] Revised—December 2008
198:

Hereditary Renal Hypouricemia, [Abstract] [Full Text]
198S:

Hereditary Renal Hypouricemia: Identification of the Gene Defect in Hereditary Renal Hypouricemia, Oded Sperling [Abstract] [Full Text] Supplement—January 2008
199:

Cystinosis: A Disorder of Lysosomal Membrane Transport, William A. Gahl / Jess G. Thoene / Jerry A. Schneider [Abstract] [Full Text]
200:

Disorders of Free Sialic Acid Storage, [Abstract] [Full Text]
200S:

Recent Developments in Disorders of Free Sialic Acid Storage, Pertti Aula / Nina Aula / William A. Gahl [Abstract] [Full Text]
201:

Cystic Fibrosis, Garry R. Cutting / Frank Accurso / Bonnie W. Ramsey / Michael J. Welsh [Abstract] [Full Text]
202:

Defects in Sulfate Metabolism and Skeletal Dysplasias, Andrea Superti-Furga [Abstract] [Full Text]
203:

Familial Cardiac Arrhythmias, Mark T. Keating / Michael C. Sanguinetti [Abstract] [Full Text]
204:

Channelopathies: Episodic Disorders of the Nervous System, Joanna Jen / Louis Ptáček [Abstract] [Full Text]