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1دورية أكاديمية
المؤلفون: Takashi Sakoh, Akinari Sekine, Takayasu Mori, Hiroki Mizuno, Masahiro Kawada, Rikako Hiramatsu, Eiko Hasegawa, Noriko Hayami, Masayuki Yamanouchi, Tatsuya Suwabe, Naoki Sawa, Yoshifumi Ubara, Takuya Fujimaru, Eisei Sohara, Uchida Shinichi, Junichi Hoshino, Kenmei Takaichi
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
مصطلحات موضوعية: D564N, familial case, pseudohypoaldosteronism type II, WNK4, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269
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2
المؤلفون: Masayuki Yamanouchi, Uchida Shinichi, Kenmei Takaichi, Hiroki Mizuno, Noriko Hayami, Takashi Sakoh, Eiko Hasegawa, Tatsuya Suwabe, Yoshifumi Ubara, Naoki Sawa, Takuya Fujimaru, Masahiro Kawada, Takayasu Mori, Rikako Hiramatsu, Akinari Sekine, Junichi Hoshino, Eisei Sohara
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicineمصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Trichlormethiazide, Hyperkalemia, lcsh:QH426-470, Pseudohypoaldosteronism, Amino Acid Motifs, Mutation, Missense, Anion gap, 030105 genetics & heredity, Protein Serine-Threonine Kinases, Excretion, 03 medical and health sciences, pseudohypoaldosteronism type II, D564N, WNK4, Internal medicine, Genetics, medicine, Missense mutation, Humans, Diuretics, Molecular Biology, Genetics (clinical), Antihypertensive Agents, Kidney, business.industry, Original Articles, medicine.disease, Urinary calcium, Pedigree, lcsh:Genetics, 030104 developmental biology, Endocrinology, medicine.anatomical_structure, Phenotype, Female, Original Article, medicine.symptom, business, familial case, medicine.drug