Cargando…
Hereditary intrinsic factor deficiency in China caused by a novel mutation in the intrinsic factor gene—a case report
BACKGROUND: Hereditary intrinsic factor deficiency is a rare disease characterized by cobalamin deficiency with the lack of gastric intrinsic factor because of gastric intrinsic factor (GIF) mutations. Patients usually present with cobalamin deficiency without gastroscopy abnormality and intrinsic f...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654184/ https://www.ncbi.nlm.nih.gov/pubmed/33172407 http://dx.doi.org/10.1186/s12881-020-01158-z |