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Article

A Novel Mutation of Notch homolog protein 2 gene in a Chinese Family with Hajdu-Cheney Syndrome.

Chinese medical journal - 5 Dec 2017

Gong Ruo-Lan, Wu Jing, Chen Tong-Xin

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 29176149
DOI: 10.4103/0366-6999.219141
PMCID: PMC5717871

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Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.Semantic proximity Read ↗

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