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Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene150

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Μάρτιος 2024Απρίλιος 2024Μάϊος 2024Ιούνιος 2024Ιούλιος 2024Αύγουστος 2024Σεπτέμβριος 2024
Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene0037485

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