Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.
about
Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism.Pseudohypoaldosteronism in a neonate presenting as life-threatening arrhythmia.Effect of NR3C2 genetic polymorphisms on the blood pressure response to enalapril treatment.
P2860
Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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2011年论文
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name
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@ast
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@en
type
label
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@ast
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@en
prefLabel
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@ast
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@en
P2093
P2860
P356
P1476
Mineralocorticoid receptor mut ...... seudohypoaldosteronism type 1.
@en
P2093
Brigitte Escoubet
Chantal Metz
Edwige-Ludiwyne Hubert
Fábio L Fernandes-Rosa
Maria-Christina Zennaro
Marie-Edith Rafestin-Oblin
Michel Fay
Raphaël Teissier
P2860
P304
P356
10.1681/ASN.2011030245
P577
2011-09-08T00:00:00Z