A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-1203
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
-
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism ; day:25 ; month:4 ; year:2017 ; pages:1-11
Human genetics; (25.4.2017), 1-11
- Schlagwort
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Erbkrankheit
Erbschaden
- Urheber
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Pillar, Nir
- Beteiligte Personen und Organisationen
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Pleniceanu, Oren
Fang, Mingyan
Ziv, Limor
Lahav, Einat
Botchan, Shay
Cheng, Le
Dekel, Benjamin
Shomron, Noam
SpringerLink (Online service)
- DOI
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10.1007/s00439-017-1804-9
- URN
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urn:nbn:de:1111-2017050712282
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Beteiligte
- Pillar, Nir
- Pleniceanu, Oren
- Fang, Mingyan
- Ziv, Limor
- Lahav, Einat
- Botchan, Shay
- Cheng, Le
- Dekel, Benjamin
- Shomron, Noam
- SpringerLink (Online service)
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