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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 gene

✍ Scribed by M Feldman; M Prikis; Y Athanasiou; A Elia; A Pierides; CC Deltas


Book ID
110888155
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
427 KB
Volume
69
Category
Article
ISSN
0009-9163

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