Your browser doesn't support javascript.
loading
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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-33172407

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina B 12 / Deficiência de Vitamina B 12 / Mutação da Fase de Leitura / Fator Intrínseco / Anemia Perniciosa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina B 12 / Deficiência de Vitamina B 12 / Mutação da Fase de Leitura / Fator Intrínseco / Anemia Perniciosa Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article