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A Novel PHEX Gene Mutation in a Patient with Sporadic Hypophosphatemic Rickets
Yea Eun Kang, Jun Hwa Hong, Jimin Kim, Kyong Hye Joung, Hyun Jin Kim, Bon Jeong Ku, Koon Soon Kim
Endocrinol Metab. 2014;29(2):195-201.   Published online June 26, 2014
DOI: https://doi.org/10.3803/EnM.2014.29.2.195

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A NovelPHEXGene Mutation in a Patient with Sporadic Hypophosphatemic Rickets
Endocrinology and Metabolism. 2014;29(2):195   Crossref logo
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Novel PHEX Gene Mutation Associated with X Linked Hypophosphatemic Rickets
Nephron Physiology. 2010;116(3):p17-p21   Crossref logo
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Identification a novel insertion PHEX mutation in a sporadic patient with hypophosphatemic rickets
Journal of Endocrinological Investigation. 2018;42(3):357-359   Crossref logo
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SAT-373 A Case of X Linked Hypophosphatemic Rickets Due to DE Novo Phex Gene Mutation
Journal of the Endocrine Society. 2020;4(Supplement_1):   Crossref logo
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Novel PHEX Mutation Associated with Hypophosphatemic Rickets
Nephron Physiology. 2007;106(1):p8-p12   Crossref logo
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Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic rickets
Human Mutation. 2000;15(4):383-384   Crossref logo
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A novel mutation of PHEX causes a dominant X-linked hypophosphatemic rickets
Bone. 2007;40(6):S62   Crossref logo
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Mutational analysis of PHEX, FGF23 and DMP1 in a cohort of patients with hypophosphatemic rickets
Clinical Endocrinology. 2011;74(3):312-318   Crossref logo
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A novel de novo mosaic mutation in PHEX in a Korean patient with hypophosphatemic rickets
Annals of Pediatric Endocrinology & Metabolism. 2018;23(4):229-234   Crossref logo
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A NovelPHEXMutation in Japanese Patients with X-Linked Hypophosphatemic Rickets
Case Reports in Genetics. 2015;2015:1-5   Crossref logo
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