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Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update.

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Title: Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update.
Authors: Schätzl, Teresa1 (AUTHOR), Kaiser, Lars1,2 (AUTHOR), Deigner, Hans-Peter1,3,4 (AUTHOR) hans-peter.deigner@hs-furtwangen.de
Source: Orphanet Journal of Rare Diseases. 3/12/2021, Vol. 16 Issue 1, p1-26. 26p.
Database: Academic Search Ultimate
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  Data: Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 3/12/2021, Vol. 16 Issue 1, p1-26. 26p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=149248100
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      – Type: doi
        Value: 10.1186/s13023-021-01760-1
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      – Code: eng
        Text: English
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        PageCount: 26
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      – TitleFull: Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update.
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            NameFull: Schätzl, Teresa
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            NameFull: Kaiser, Lars
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            NameFull: Deigner, Hans-Peter
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              Text: 3/12/2021
              Type: published
              Y: 2021
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