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CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.

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Title: CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.
Authors: Gidaro, T.1, Vandenbrande, L.1, Malfatti, E.1, Labasse, C.1, Carlier, P.1, Romero, N.1, Servais, L.1, Böhm, J.2
Source: Neuromuscular Disorders. Oct2018:Supplement 2, Vol. 28, pS51-S51. 1p.
Database: Academic Search Ultimate
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Header DbId: asn
DbLabel: Academic Search Ultimate
An: 131609078
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.
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  Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Oct2018:Supplement 2, Vol. 28, pS51-S51. 1p.
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RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1016/j.nmd.2018.06.098
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      – Code: eng
        Text: English
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        PageCount: 1
        StartPage: S51
    Titles:
      – TitleFull: CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.
        Type: main
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            NameFull: Gidaro, T.
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            NameFull: Malfatti, E.
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            NameFull: Labasse, C.
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            NameFull: Carlier, P.
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            NameFull: Romero, N.
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            NameFull: Servais, L.
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            NameFull: Böhm, J.
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            – D: 02
              M: 10
              Text: Oct2018:Supplement 2
              Type: published
              Y: 2018
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              Value: 09608966
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              Value: 28
          Titles:
            – TitleFull: Neuromuscular Disorders
              Type: main
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