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Home > Publications database > A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life > Access to Fulltext
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A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life - FZJ-2022-01412
 
Main document file(s):
      521626
    version 1
    521626.pdf [870.37 KB] 27 Jul 2022, 08:32 OpenAccess
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