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Volumn 14, Issue 12, 1996, Pages 1417-1419

Lack of mutations in epithelial sodium channel β-subunit gene in human subjects with hypertension

Author keywords

Epithelial sodium channel; Genetic diagnosis; Genetic mutation; Hypertension

Indexed keywords

SODIUM CHANNEL;

EID: 0030444762     PISSN: 02636352     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004872-199612000-00005     Document Type: Article
Times cited : (34)

References (11)
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  • 2
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  • 4
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    • Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1
    • Chang SS, Grunder S, Hanukoglu A, Roesler A, Mathew PM, Hanukoglu I. et al.: Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nature Genet 1996, 12:248-253.
    • (1996) Nature Genet , vol.12 , pp. 248-253
    • Chang, S.S.1    Grunder, S.2    Hanukoglu, A.3    Roesler, A.4    Mathew, P.M.5    Hanukoglu, I.6
  • 5
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    • A novel splice-site mutation in the γ subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families
    • Strautnieks SS, Thompson RJ, Gardiner RM, Chung E: A novel splice-site mutation in the γ subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families. Nature Genet 1996, 13:248-250.
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    • Strautnieks, S.S.1    Thompson, R.J.2    Gardiner, R.M.3    Chung, E.4
  • 6
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    • Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
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    • Shimkets, R.A.1    Warnock, D.G.2    Bositis, C.M.3    Nelson-Williams, C.4    Hansson, J.H.5    Schambelan, M.6
  • 7
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  • 8
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    • Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated NaI and SDS
    • Wang L, Hirayasu K, Ishizawa M, Kobayashi Y: Purification of genomic DNA from human whole blood by isopropanol-fractionation with concentrated NaI and SDS. Nucl Acids Res 1994, 22:1774-1775.
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    • Hypertension caused by a truncated epithelial sodium channel γ subunit: Genetic heterogeneity of Liddle syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.