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The Application of Clinical Genetics Volume 13, 2020 - Issue
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Case report

PHEX Gene Mutation in a Patient with X-Linked Hypophosphatemic Rickets in a Developing Country

Jessica María Forero-Delgadillo1 Pediatric Nephrology Fellow, Universidad Icesi-Fundación Valle de Lili, Cali, Colombia;2 Facultad de Ciencias de la Salud, Universidad Icesi, Cali, ColombiaORCID Iconhttps://orcid.org/0000-0002-6526-757X
ORCID Icon,
Daniela Cleves2 Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia;3 Pediatrics Resident, Universidad Icesi-Fundación Valle de Lili, Cali, ColombiaORCID Iconhttps://orcid.org/0000-0001-7321-2045
ORCID Icon,
Vanessa Ochoa1 Pediatric Nephrology Fellow, Universidad Icesi-Fundación Valle de Lili, Cali, Colombia;2 Facultad de Ciencias de la Salud, Universidad Icesi, Cali, ColombiaORCID Iconhttps://orcid.org/0000-0003-1944-2776
ORCID Icon,
Hernando Londoño-Correa4 Pediatric Nephrology Department, Fundación Valle del Lili, Cali, Colombia
,
Jaime Manuel Restrepo4 Pediatric Nephrology Department, Fundación Valle del Lili, Cali, Colombia
,
José Antonio Nastasi-Catanese4 Pediatric Nephrology Department, Fundación Valle del Lili, Cali, Colombia;5 Clinical Genetics Department, Fundación Valle del Lili, Cali, ColombiaORCID Iconhttps://orcid.org/0000-0001-9078-1127
ORCID Icon &
Harry Pachajoa2 Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia;5 Clinical Genetics Department, Fundación Valle del Lili, Cali, ColombiaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0003-2672-0439
ORCID Icon show all
Pages 57-62 | Published online: 13 Feb 2020

References

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