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New mutation in FOXP3 gene identified in an infant with chronic diarrhea as manifestation of autoinmune enteropathy - IPEX syndrome.

Overview of attention for article published in Revista chilena de pediatría, August 2020
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Title
New mutation in FOXP3 gene identified in an infant with chronic diarrhea as manifestation of autoinmune enteropathy - IPEX syndrome.
Published in
Revista chilena de pediatría, August 2020
DOI 10.32641/rchped.v91i4.1467
Pubmed ID
Authors

Clara Plata García, Lorena Martín-Marín, Angela Soler-Ramírez, Jorge A Rojas, María P Salazar

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 12 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 17%
Researcher 1 8%
Student > Master 1 8%
Unknown 8 67%
Readers by discipline Count As %
Medicine and Dentistry 3 25%
Unknown 9 75%