Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China

Overview of attention for article published in BMC Pediatrics, October 2014

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So far, Dimensions has found 24 publications that cite this research output.

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Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review

Article in Frontiers in Endocrinology (March 2024)

Epidemiological characteristics of patients with Hutchinson-Gilford progeria syndrome and progeroid laminopathies in China

Article in Pediatric Research (January 2024)

Lipodystrophy as a target to delay premature aging

Article in Trends in Endocrinology and Metabolism (November 2023)

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