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Discordant genotype-phenotype correlation in familial hyperaldosteronism type III with KCNJ5 gene mutation: a patient report and review of the literature.
Adachi, Masanori; Muroya, Koji; Asakura, Yumi; Sugiyama, Kenji; Homma, Keiko; Hasegawa, Tomonobu.
Affiliation
  • Adachi M; Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.
Horm Res Paediatr ; 82(2): 138-42, 2014.
Article in En | MEDLINE | ID: mdl-24819081
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyuria / Mutation, Missense / G Protein-Coupled Inwardly-Rectifying Potassium Channels Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Horm Res Paediatr Journal subject: ENDOCRINOLOGIA / PEDIATRIA Year: 2014 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyuria / Mutation, Missense / G Protein-Coupled Inwardly-Rectifying Potassium Channels Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Horm Res Paediatr Journal subject: ENDOCRINOLOGIA / PEDIATRIA Year: 2014 Document type: Article Affiliation country: Country of publication: