Your browser doesn't support javascript.
loading
Functional Characterization of PHEX Gene Variants in Children With X-Linked Hypophosphatemic Rickets Shows No Evidence of Genotype-Phenotype Correlation.
Zheng, Bixia; Wang, Chunli; Chen, Qiuxia; Che, Ruochen; Sha, Yugen; Zhao, Fei; Ding, Guixia; Zhou, Wei; Jia, Zhanjun; Huang, Songming; Chen, Ying; Zhang, Aihua.
Afiliación
  • Zheng B; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Wang C; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Chen Q; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Che R; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Sha Y; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Zhao F; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Ding G; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Zhou W; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Jia Z; Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Huang S; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
  • Chen Y; Jiangsu Key Laboratory of Pediatrics, Nanjing Medical University, Nanjing, China.
  • Zhang A; Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.
J Bone Miner Res ; 35(9): 1718-1725, 2020 09.
Article en En | MEDLINE | ID: mdl-32329911
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Raquitismo Hipofosfatémico Familiar Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Raquitismo Hipofosfatémico Familiar Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2020 Tipo del documento: Article País de afiliación: China