Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MRgene

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2369

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MRgene ; volume:10 ; number:1 ; day:14 ; month:11 ; year:2009 ; pages:1-6 ; date:12.2009
BMC nephrology ; 10, Heft 1 (14.11.2009), 1-6, 12.2009

Creator: Kanda, Kyoko

Contributor: Nozu, Kandai
Yokoyama, Naoki
Morioka, Ichiro
Miwa, Akihiro
Hashimura, Yuya
Kaito, Hiroshi
Iijima, Kazumoto
Matsuo, Masafumi
SpringerLink (Online service)

DOI: 10.1186/1471-2369-10-37

URN: urn:nbn:de:1111-2016081219539

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:50 AM CEST

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Associated

Kanda, Kyoko
Nozu, Kandai
Yokoyama, Naoki
Morioka, Ichiro
Miwa, Akihiro
Hashimura, Yuya
Kaito, Hiroshi
Iijima, Kazumoto
Matsuo, Masafumi
SpringerLink (Online service)

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Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MRgene

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Other Objects (12)

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A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia

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A novel MYO6 splice site mutation causes autosomal dominant sensorineural hearing loss type DFNA22 with a favourable outcome after cochlear implantation

Novel SOX2 mutation in autosomal dominant cataract-microcornea syndrome

A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia

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