bibliographic entry 12697258 [be/12697258]
https://w3id.org/oc/corpus/be/12697258

is a
content
  • Bogazzi, F, Raggi, F, Ultimieri, F. A novel mutation in the pendrin gene associated with Pendred's syndrome, Clin. Endocrinol, 52, 2000, 279, 285
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