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Nature Genetics|September 6, 2000
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearingA N Smith, J Skaug, K A Choate, et al.Science (New York, N.Y.)|July 3, 1999
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorptionD B Simon, Y Lu, K A Choate, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 8, 2016
Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatmentD Ovejero, Y H Lim, A M Boyce, et al.Science (New York, N.Y.)|August 11, 2001
Human hypertension caused by mutations in WNK kinasesF H Wilson, S Disse-Nicodème, K A Choate, et al.Pageof 2