Risk and Clinical Significance of Idiopathic Preterm Birth in Microvillus Inclusion Disease

Microvillus inclusion disease (MVID) is a rare enteropathy caused by mutations in the MYO5B or STX3 gene. MVID is a disease that is difficult to manage with clinical heterogeneity. Therefore, knowledge about factors influencing MVID morbidity and mortality is urgently needed. Triggered by a recent s...

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Detalles Bibliográficos
Autores principales: Leng, Changsen, Sun, Yue, van IJzendoorn, Sven C. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432107/
https://www.ncbi.nlm.nih.gov/pubmed/34501384
http://dx.doi.org/10.3390/jcm10173935

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8432107/
https://www.ncbi.nlm.nih.gov/pubmed/34501384
http://dx.doi.org/10.3390/jcm10173935

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