The FSHD2 Gene <em>SMCHD1</em> Is a Modifier of Disease Severity in Families Affected by FSHD1期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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*The FSHD2 Gene SMCHD1* Is a Modifier of Disease Severity in Families Affected by FSHD1**

Authors:	Sabrina Sacconi Richard JLF Lemmers Judit Balog Patrick J van der Vliet Pauline Lahaut Merlijn P van Nieuwenhuizen Kirsten R Straasheijm Rashmie D Debipersad Marianne Vos-Versteeg Leonardo Salviati Alberto Casarin Elena Pegoraro Rabi Tawil Egbert Bakker Stephen J Tapscott Claude Desnuelle Silvère M van der Maarel

Institution:	¹ Neuromuscular Diseases Centre, University Hospital of Nice, 06000 Nice, France;² CNRS UMR7277, IBV, Faculty of Medicine, University of Nice, 06108 Nice, France;³ Department of Human Genetics, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands;⁴ Department of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands;⁵ Clinical Genetics Unit, Department of Woman and Child Health, University of Padova, 35128 Padova, Italy;⁶ Instituto di Ricerca Pediatrica, Città della Speranza, 35128 Padova, Italy;⁷ Department of Neurosciences, NPSRR, University of Padova, 35128 Padova, Italy;⁸ Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA;⁹ Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA

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