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2. X-linked recessive nephrolithiasis with renal failure;Frymoyer;N Engl J Med,1991
3. Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets;Bolino;Eur J Hum Genet,1993
4. Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis;Akuta;Kidney Int,1997
5. Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease;Igarashi;Kidney Int,1998