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Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene
Boualla, L., Jdioui, W., Soulami, K., Ratbi, I., Sefiani, A.Language:
english
Journal:
Current Research in Translational Medicine
DOI:
10.1016/j.retram.2016.01.005
Date:
February, 2016
File:
PDF, 602 KB
english, 2016