Á lódáil...
Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene
BACKGROUND: Congenital lactase deficiency (CLD) is a rare severe autosomal recessive disorder, with symptoms like watery diarrhea, meteorism and malnutrition, which start a few days after birth by the onset of nursing. The most common rationales identified for this disorder are missense mutations or...
Na minha lista:
| Foilsithe in: | BMC Gastroenterol |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BioMed Central
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4432517/ https://ncbi.nlm.nih.gov/pubmed/25881162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12876-015-0261-y |
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