The article by Monkawa et al., "Novel Mutation in
Thiazide-SensitiveNa-Cl Cotransporter Gene of Patients with Gitelman's
Syndrome"(J Am Soc Nephrol
11: 65-70, 2000) contained an error in theamino acid substitution
caused by a mutation. In patient E,the C-T amino acid change caused the
mutation Ala569Val, ratherthan Ala569Glu. As a result, the following
corrections shouldbe noted: (1) In the Abstract, column 2, line 9,
"Ala569Glu"should read "Ala569Val." (2) In
Table 1, "A569E" should read"A569V." (3) In
the Results section, p. 68, column 2, lines22 and 25, "Ala to
Glu" should read "Ala to Val"; p. 69, column1, line 1, and
p. 70, column 1, lines 5 and 7, "Ala569Glu" shouldread
"Ala569Val." (4) In Figure 4 legend, "Ala to
Glu" shouldread "Ala to Val." The authors regret any
inconvenience causedby this error.
In the article "The Luminal P2Y Receptor in the Isolated Perfused
MouseCortical Collecting Duct," by P. Deetjen, J. Thomas, H. Lehrmann,
S.J. Kim, and J. Leipziger (J Am
Soc Nephrol 11: 1798-1806, 2000),P. Deetjen and J. Thomas
contributed equally to the work.
