Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy

S. Pasteuning-Vuhman; K. Putker; C. L. Tanganyika-de Winter; J. W. Boertje-van der Meulen; L. van Vliet; M. Overzier; J. J. Plomp; A. Aartsma-Rus; M. van Putten

doi:10.1371/journal.pone.0197388

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Open Access

Peer-reviewed

Research Article

Natural disease history of the dy^2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy

S. Pasteuning-Vuhman,

Roles Formal analysis, Investigation, Validation, Visualization, Writing – original draft

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
K. Putker,

Roles Data curation, Formal analysis, Investigation

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
C. L. Tanganyika-de Winter,

Roles Data curation

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
J. W. Boertje-van der Meulen,

Roles Data curation

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
L. van Vliet,

Roles Data curation

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
M. Overzier,

Roles Data curation

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
J. J. Plomp,

Roles Conceptualization, Data curation, Formal analysis, Investigation, Writing – review & editing

Affiliation Department of Neurology Leiden University Medical Centre, Leiden, The Netherlands
⨯
A. Aartsma-Rus,

Roles Conceptualization, Funding acquisition, Investigation, Supervision, Writing – review & editing

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯
M. van Putten

Roles Conceptualization, Data curation, Funding acquisition, Investigation, Supervision, Validation, Writing – review & editing

* E-mail: M.van_Putten@lumc.nl

Affiliation Department of Human Genetics Leiden University Medical Centre, Leiden, The Netherlands
⨯

Natural disease history of the dy^2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy

S. Pasteuning-Vuhman,
K. Putker,
C. L. Tanganyika-de Winter,
J. W. Boertje-van der Meulen,
L. van Vliet,
M. Overzier,
J. J. Plomp,
A. Aartsma-Rus,
M. van Putten

Published: May 15, 2018
https://doi.org/10.1371/journal.pone.0197388

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