A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6 ; volume:6 ; number:1 ; day:6 ; month:3 ; year:2019 ; pages:1-3 ; date:12.2019
Human genome variation ; 6, Heft 1 (6.3.2019), 1-3, 12.2019
- Creator
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Goda, Takeshi
Komatsu, Hiroshi
Nozu, Kandai
Nakajima, Hisakazu
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41439-019-0043-0
- URN
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urn:nbn:de:101:1-2019033123171672930188
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Goda, Takeshi
- Komatsu, Hiroshi
- Nozu, Kandai
- Nakajima, Hisakazu
- SpringerLink (Online service)
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