CrossRef Text and Data Mining
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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

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

The Application of Clinical Genetics. 2020;Volume 13:57-62   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 Phex mutation in a new mouse model of hypophosphatemic rickets
Journal of Cellular Biochemistry. 2012;113(7):2432-2441   Crossref logo
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Novel de novo nonsense mutation of the PHEX gene (p.Lys50Ter) in a Chinese patient with hypophosphatemic rickets
Gene. 2015;565(1):150-154   Crossref logo
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Identification of a novel loss-of-function PHEX mutation, Ala720Ser, in a sporadic case of adult-onset hypophosphatemic osteomalacia
Bone. 2018;106:30-34   Crossref logo
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