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家族性先天性心疾患における染色体22q11内の欠損

D I Wilson1, J A Goodship, J Burn

  • 1Division of Human Genetics, University of Newcastle upon Tyne, UK.

Lancet (London, England)
|September 5, 1992
PubMed
まとめ

染色体22の欠損は,ディジョージ症候群とシュプリンテン症候群に関連しており,しばしば心不全を引き起こす. この研究では,遺伝的な心臓疾患を持つ家族でこれらの削除が発見され,重要な遺伝的原因が示唆されています.

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