Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

N Jeck; Christian Derst; E Wischmeyer; H Ott; S Weber; C Rudin; H W Seyberth; J Daut; A Karschin; M Konrad

doi:10.1046/j.1523-1755.2001.0590051803.x

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

N Jeck, Christian Derst (Co-Autor/-in), E Wischmeyer, H Ott, S Weber, C Rudin, H W Seyberth, J Daut, A Karschin, M Konrad

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

43 Quellenangaben (Web of Science)

Originalsprache	Englisch
Seiten (von - bis)	1803-1811
Fachzeitschrift	KIDNEY INTERNATIONAL
Jahrgang	59
Ausgabenummer	5
DOIs	https://doi.org/10.1046/j.1523-1755.2001.0590051803.x
Publikationsstatus	Veröffentlicht - 2001

Zugriff auf Dokument

10.1046/j.1523-1755.2001.0590051803.x

Dieses zitieren

Jeck, N., Derst, C., Wischmeyer, E., Ott, H., Weber, S., Rudin, C., Seyberth, H. W., Daut, J., Karschin, A., & Konrad, M. (2001). Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome. KIDNEY INTERNATIONAL , 59(5), 1803-1811. https://doi.org/10.1046/j.1523-1755.2001.0590051803.x

Jeck, N ; Derst, Christian ; Wischmeyer, E et al. / Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome. in: KIDNEY INTERNATIONAL 2001 ; Jahrgang 59, Nr. 5. S. 1803-1811.

@article{ee826d664337455b9efea8bee071da74,

title = "Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.",

keywords = "ANTENATAL BARTTER-SYNDROME, RECTIFIER K+ CHANNEL, POTASSIUM CHANNEL, GENETIC-HETEROGENEITY, CLONING, HYPERCALCIURIA, MECHANISMS, EXPRESSION, TRANSPORT, VARIANT",

author = "N Jeck and Christian Derst and E Wischmeyer and H Ott and S Weber and C Rudin and Seyberth, \{H W\} and J Daut and A Karschin and M Konrad",

year = "2001",

doi = "10.1046/j.1523-1755.2001.0590051803.x",

language = "English",

volume = "59",

pages = "1803--1811",

journal = "KIDNEY INTERNATIONAL ",

issn = "0085-2538",

number = "5",

}

Jeck, N, Derst, C, Wischmeyer, E, Ott, H, Weber, S, Rudin, C, Seyberth, HW, Daut, J, Karschin, A & Konrad, M 2001, 'Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.', KIDNEY INTERNATIONAL , Jg. 59, Nr. 5, S. 1803-1811. https://doi.org/10.1046/j.1523-1755.2001.0590051803.x

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome. / Jeck, N; Derst, Christian (Co-Autor/-in); Wischmeyer, E et al.
in: KIDNEY INTERNATIONAL , Jahrgang 59, Nr. 5, 2001, S. 1803-1811.

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

TY - JOUR

T1 - Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

AU - Jeck, N

AU - Derst, Christian

AU - Wischmeyer, E

AU - Ott, H

AU - Weber, S

AU - Rudin, C

AU - Seyberth, H W

AU - Daut, J

AU - Karschin, A

AU - Konrad, M

PY - 2001

Y1 - 2001

KW - ANTENATAL BARTTER-SYNDROME

KW - RECTIFIER K+ CHANNEL

KW - POTASSIUM CHANNEL

KW - GENETIC-HETEROGENEITY

KW - CLONING

KW - HYPERCALCIURIA

KW - MECHANISMS

KW - EXPRESSION

KW - TRANSPORT

KW - VARIANT

U2 - 10.1046/j.1523-1755.2001.0590051803.x

DO - 10.1046/j.1523-1755.2001.0590051803.x

M3 - Original Article

C2 - 11318951

SN - 0085-2538

VL - 59

SP - 1803

EP - 1811

JO - KIDNEY INTERNATIONAL

JF - KIDNEY INTERNATIONAL

IS - 5

ER -

Jeck N, Derst C, Wischmeyer E, Ott H, Weber S, Rudin C et al. Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome. KIDNEY INTERNATIONAL . 2001;59(5):1803-1811. doi: 10.1046/j.1523-1755.2001.0590051803.x