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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432517/ https://www.ncbi.nlm.nih.gov/pubmed/25881162 http://dx.doi.org/10.1186/s12876-015-0261-y |