Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency

Congenital sucrase-isomaltase deficiency (CSID) is an autosomal recessive disorder of carbohydrate maldigestion and malabsorption caused by mutations in the sucrase-isomaltase (SI) gene. SI, together with maltase-glucoamylase (MGAM), belongs to the enzyme family of disaccharidases required for break...

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Detalles Bibliográficos
Autores principales: Husein, Diab M., Wanes, Dalanda, Marten, Lara M., Zimmer, Klaus-Peter, Naim, Hassan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Concept Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835860/
https://www.ncbi.nlm.nih.gov/pubmed/31557950
http://dx.doi.org/10.3390/nu11102290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835860/
https://www.ncbi.nlm.nih.gov/pubmed/31557950
http://dx.doi.org/10.3390/nu11102290

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