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LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family

Detalles Bibliográficos
Autores principales:	Nunes, D, Nogueira, C, Lopes, A, Chaves, P, Rodrigues, E, Cardoso, T, Leão Teles, E, Vilarinho, L
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2016
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050266/ https://www.ncbi.nlm.nih.gov/pubmed/27722093 http://dx.doi.org/10.1016/j.ymgmr.2016.09.004

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