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Detalhes Referência

Tipo
Artigos em Revista

Tipo de Documento
Artigo Completo

Título
Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy

Participantes na publicação
Andreia M. Nunes (Author)
FACULDADE DE CIÊNCIAS DA UNIVERSIDADE DE LISBOA
Ryan D. Wuebbles (Author)
Apurva Sarathy (Author)
Tatiana M. Fontelonga (Author)
Marianne Deries (Author)
FACULDADE DE CIÊNCIAS DA UNIVERSIDADE DE LISBOA
Dean J. Burkin (Author)
Sólveig Thorsteinsdóttir (Author)
Dep. Biologia Animal
cE3c

Data de Publicação
2017-03-07

Suporte
Human Molecular Genetics

Identificadores da Publicação
ISSN - 0964-6906

Editora
Oxford University Press (OUP)

Volume
26
Fascículo
11

Página Inicial
2018
Página Final
2033

Identificadores do Documento
URL - http://dx.doi.org/10.1093/hmg/ddx083
DOI - https://doi.org/10.1093/hmg/ddx083

Identificadores de Qualidade
Web Of Science Q1 (2017) - 4.902 - GENETICS & HEREDITY - SCIE


Exportar referência

APA
Andreia M. Nunes, Ryan D. Wuebbles, Apurva Sarathy, Tatiana M. Fontelonga, Marianne Deries, Dean J. Burkin, Sólveig Thorsteinsdóttir, (2017). Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy. Human Molecular Genetics, 26, 2018-2033. ISSN 0964-6906. eISSN . http://dx.doi.org/10.1093/hmg/ddx083

IEEE
Andreia M. Nunes, Ryan D. Wuebbles, Apurva Sarathy, Tatiana M. Fontelonga, Marianne Deries, Dean J. Burkin, Sólveig Thorsteinsdóttir, "Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy" in Human Molecular Genetics, vol. 26, pp. 2018-2033, 2017. 10.1093/hmg/ddx083

BIBTEX
@article{36518, author = {Andreia M. Nunes and Ryan D. Wuebbles and Apurva Sarathy and Tatiana M. Fontelonga and Marianne Deries and Dean J. Burkin and Sólveig Thorsteinsdóttir}, title = {Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy}, journal = {Human Molecular Genetics}, year = 2017, pages = {2018-2033}, volume = 26 }