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doi: 10.1016/0026-0495(77)90101-9 17 SinclairCGilchristJMHennesseyJVKandulaM
Jede Charge wird unabhngig im Labor geprft und dokumentiert
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town
Biochim Biophys Acta Mol Basis Dis
