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Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives
Congenital lactase deficiency (CLD) is a severe autosomal recessive genetic disorder that affects the functional capacity of the intestinal protein lactase-phlorizin hydrolase (LPH). This disorder is diagnosed already during the first few days of the newborn’s life due to the inability to digest lac...
Shranjeno v:
| izdano v: | Nutrients |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6412902/ https://ncbi.nlm.nih.gov/pubmed/30813293 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/nu11020461 |
| Oznake: |
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