Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1435-232X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis ; day:16 ; month:12 ; year:2022 ; pages:1-4
Journal of human genetics ; (16.12.2022), 1-4

Creator: Udupa, Prajna
Ghosh, Debasish Kumar
Kausthubham, Neethukrishna
Shah, Hitesh
Bartakke, Sandip
Dalal, Ashwin
Girisha, Katta M.
Bhavani, Gandham SriLakshmi

Contributor: SpringerLink (Online service)

DOI: 10.1038/s10038-022-01104-2

URN: urn:nbn:de:101:1-2023022721030042485030

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

Last update: 14.08.2025, 10:44 AM CEST

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Associated

Udupa, Prajna
Ghosh, Debasish Kumar
Kausthubham, Neethukrishna
Shah, Hitesh
Bartakke, Sandip
Dalal, Ashwin
Girisha, Katta M.
Bhavani, Gandham SriLakshmi
SpringerLink (Online service)

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Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis

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Other Objects (12)

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