SLC10A2 deficiency‐induced congenital chronic bile acid diarrhea and stunting-Reference-Cited by-同舟云学术

SLC10A2 deficiency‐induced congenital chronic bile acid diarrhea and stunting

Published:2021-06-30 Issue:8 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Qie Di¹,Zhang Yulin¹,Gong Xue¹,He Yunru¹,Qiao Lina¹,Lu Guoyan¹,Li Yifei¹^ORCID

Affiliation:

1. Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE Department of Pediatrics Sichuan University Chengdu Sichuan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1740

Reference26 articles.

1. The Receptor TGR5 Mediates the Prokinetic Actions of Intestinal Bile Acids and Is Required for Normal Defecation in Mice

2. Bile Acid Diarrhea: Prevalence, Pathogenesis, and Therapy

3. Editorial: Dissecting Molecular Mechanisms in Bile Acid Diarrhea

4. Genetic variation in GPBAR1 predisposes to quantitative changes in colonic transit and bile acid excretion

5. The SLC10 Carrier Family

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