Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia ; volume:10 ; number:1 ; day:26 ; month:1 ; year:2023 ; pages:1-3 ; date:12.2023
Human genome variation ; 10, Heft 1 (26.1.2023), 1-3, 12.2023

Creator: Adachi, Junya
Aoki, Yoshihiko
Izumi, Hiroto
Nishiyama, Takeshi
Nakayama, Atsuo
Sana, Masatoshi
Morimoto, Kyoko
Kaetsu, Atsuo
Shirozu, Takamasa
Osumi, Eriko
Matsuoka, Michiko
Hayakawa, Eri
Maeda, Nasel
Machida, Junichiro
Nagao, Toru
Tokita, Yoshihito

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41439-023-00230-3

URN: urn:nbn:de:101:1-2024032510165381080248

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:47 AM CEST

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Associated

Adachi, Junya
Aoki, Yoshihiko
Izumi, Hiroto
Nishiyama, Takeshi
Nakayama, Atsuo
Sana, Masatoshi
Morimoto, Kyoko
Kaetsu, Atsuo
Shirozu, Takamasa
Osumi, Eriko
Matsuoka, Michiko
Hayakawa, Eri
Maeda, Nasel
Machida, Junichiro
Nagao, Toru
Tokita, Yoshihito
SpringerLink (Online service)

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Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia

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Other Objects (12)

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A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case

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A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

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A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family

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