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Chloride channel mutations in hypercalciuric kidney stone disease

✍ Scribed by Rajesh V. Thakker

Publisher
Springer
Year
1998
Tongue
English
Weight
522 KB
Volume
2
Category
Article
ISSN
1342-1751

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## Communicated by Jurgen Horst Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal-and liverrelated morbidity and mortality. The clinical spectrum is widely variable. About 30 to 50% of affected individuals die in the neonatal period, while others survive