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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...

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Detalhes bibliográficos
Publicado no:Nutrients
Main Authors: Wanes, Dalanda, Husein, Diab M., Naim, Hassan Y.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2019
Assuntos:
Acesso em linha: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
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