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Autor:
Gabriela Doro scedil, Raluca Isac, Mihai Gafencu, Adela Chiri tcedil, Ramona Stroescu, acaron
Publikováno v:
Posters.
Introduction Nephrogenic diabetes insipidus is a rare X linked syndrome, secondary to mutations in the gene encoding the vasopressin V2 receptor, located at position Xq28. In infants, clinical presentation is with signs of dehydration (fever, constip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffd870d1c3c5e77fd4b9bd0e20579045
https://doi.org/10.1136/archdischild-2017-313273.183
https://doi.org/10.1136/archdischild-2017-313273.183
