A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene

Detalles Bibliográficos
Autores principales: Kiratli Nalbant, Esra, Karaosmanoglu, Nermin, Kutlu, Omer, Ceylaner, Serdar, Eksioglu, Hatice Meral
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510937/
https://www.ncbi.nlm.nih.gov/pubmed/31192996
http://dx.doi.org/10.1016/j.jdcr.2019.03.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510937/
https://www.ncbi.nlm.nih.gov/pubmed/31192996
http://dx.doi.org/10.1016/j.jdcr.2019.03.008

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