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Hereditary intrinsic factor deficiency in China caused by a novel mutation in the intrinsic factor gene-a case report.
Ruan, Jing; Han, Bing; Zhuang, Junling; Chen, Miao; Chen, Fangfei; Huang, Yuzhou; Zhou, Wenzhe.
Afiliación
  • Ruan J; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
  • Han B; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China. rjgrass@126.com.
  • Zhuang J; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
  • Chen M; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
  • Chen F; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
  • Huang Y; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
  • Zhou W; Department of Hematology, Peking Union Medical College, Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
BMC Med Genet ; 21(1): 221, 2020 11 10.
Article en En | MEDLINE | ID: mdl-33172407
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vitamina B 12 / Deficiencia de Vitamina B 12 / Mutación del Sistema de Lectura / Factor Intrinseco / Anemia Perniciosa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Humans / Male País/Región como asunto: Asia Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vitamina B 12 / Deficiencia de Vitamina B 12 / Mutación del Sistema de Lectura / Factor Intrinseco / Anemia Perniciosa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Humans / Male País/Región como asunto: Asia Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: China