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Article

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

Acta dermato-venereologica - 4 Jan 2017

Youssefian Leila, Vahidnezhad Hassan, Aghighi Yahya, Ziaee Vahid, Zeinali Sirous, Abiri Maryam, Uitto Jouni

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27174544
DOI: 10.2340/00015555-2459

Genes

ANTXR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.PMID 27174544Read ↗

Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India.Semantic proximity Read ↗

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Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.Semantic proximity Read ↗

Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation.Semantic proximity Read ↗

[Analysis of pathogenic variants in a Chinese pedigree affected with hyaline fibromatosis syndrome].Semantic proximity Read ↗

Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene.Semantic proximity Read ↗

[Identification of novel compound heterozygous mutations in the ANTXR2 gene in a Chinese patient with juvenile hyaline fibromatosis].Semantic proximity Read ↗

Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.Semantic proximity Read ↗

Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.Semantic proximity Read ↗

Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene.Semantic proximity Read ↗

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