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Article

AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia

14 Aug 2023

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37582359
DOI: 10.1016/j.ajhg.2023.07.011

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Related research

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AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasiaPMID 37582359Read ↗

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AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.Semantic proximity Read ↗

An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family.Semantic proximity Read ↗

Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.Semantic proximity Read ↗

The structural and functional determinants of the Axin and Dishevelled DIX domains.Semantic proximity Read ↗

The links between axin and carcinogenesisSemantic proximity Read ↗

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.Semantic proximity Read ↗

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