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Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy.

Clinical genetics - 1 May 2021

McMillan Hugh J, Marshall Aren E, Venkateswaran Sunita, Hartley Taila, Warman-Chardon Jodi, Ramani Arun K, Marshall Christian R, Michaud Jean, Boycott Kym M, Dyment David A, Kernohan Kristin D

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 33576074
DOI: 10.1111/cge.13935

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

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