A novelPCLN-1gene mutation in familial hypomagnesemia with...

Pediatric Nephrology 2007 / 04 Vol. 22; Iss. 4

A novelPCLN-1gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype

Sami A. Sanjad, Ali Hariri, Zouhayr M. Habbal, Richard P. Lifton
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Volume:
22
Language:
english
Pages:
6
DOI:
10.1007/s00467-006-0354-5
Date:
April, 2007
File:
PDF, 183 KB
english, 2007
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