Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotypic parents using optical genome mapping

Overview of attention for article published in Frontiers in Neurology, February 2024

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RT @FrontNeurol: New Research: Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotyp…

02 Feb 2024

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RT @FrontNeurol: New Research: Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotyp…

01 Feb 2024

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New Research: Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotypic parents using optical genome mapping: Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is one of the… https://t.co/

01 Feb 2024

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