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Premature Aging Syndrome, Penttinen Type: Report of a Chinese Case with a PDGFRB Mutation.

Acta dermato-venereologica - 10 Oct 2018

Zhang Zhiyong, Zheng Shuguang, Zheng Song, Wang Yanyan, Xu Xue-Gang, Gao Xing-Hua, Chen Hong-Duo

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29944170
DOI: 10.2340/00015555-2993

Genes

PDGFRB

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Premature Aging Syndrome, Penttinen Type: Report of a Chinese Case with a PDGFRB Mutation.PMID 29944170Read ↗

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Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families.Semantic proximity Read ↗

Kosaki overgrowth syndrome due to a novel de novo PDGFRB variant.Semantic proximity Read ↗

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis.Semantic proximity Read ↗

Primary familial brain calcification with mild phenotype due to a new PDGFB mutation.Semantic proximity Read ↗

A Japanese family case with juvenile onset Behçet's disease caused by TNFAIP3 mutation.Semantic proximity Read ↗

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.Semantic proximity Read ↗

Ethical issues in genetics and aging: diagnosis, treatment, and prevention in the era of molecular medicine.Semantic proximity Read ↗

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