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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Detalles Bibliográficos
Autores principales: Wanes, Dalanda, Husein, Diab M., Naim, Hassan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412902/
https://www.ncbi.nlm.nih.gov/pubmed/30813293
http://dx.doi.org/10.3390/nu11020461

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412902/
https://www.ncbi.nlm.nih.gov/pubmed/30813293
http://dx.doi.org/10.3390/nu11020461

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