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Article

Progressive osseous heteroplasia in a Chinese infant and a novel mutation in the GNAS gene.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Jun 2018

Zhang S-D, Xie Z-L, Zhang K-Q, Nh-Tseung K, Zhao J-J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 29224258
DOI: 10.1111/jdv.14743

Genes

GNAS

Provenance

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Progressive osseous heteroplasia in a Chinese infant and a novel mutation in the GNAS gene.PMID 29224258Read ↗

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Progressive osseous heteroplasia in a 7-year-old girl with osteoma cutis and autoimmune thyroiditis: the importance of investigating GNAS mutations.Semantic proximity Read ↗

Progressive osseous heteroplasia in a 5-year-old boy with a novel mutation in exon 2 of GNAS: a case presentation and literature review.Semantic proximity Read ↗

Progressive osseous heteroplasia caused by a novel nonsense mutation in the GNAS1 gene.Semantic proximity Read ↗

Progressive osseous heteroplasia: diagnosis, treatment, and prognosisSemantic proximity Read ↗

Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia: first Italian series.Semantic proximity Read ↗

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