Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene

Abstract Background and aims Chronic enteropathy associated with SLCO2A1 gene is a rare intestinal disease caused by loss-of-function SLCO2A1 mutations, with clinical and genetic characteristics remaining largely unknown, especially in Chinese patients. This study aims to reveal clinical and genetic...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Orphanet Journal of Rare Diseases
المؤلفون الرئيسيون: Qing Shang, Yimin Dai, Jingyi Huang, Wei Liu, Weixun Zhou, Yaping Liu, Hong Yang, Qiang Wang, Yue Li
التنسيق: مقال
اللغة:الإنجليزية
منشور في: BMC 2024-05-01
الموضوعات:
SLCO2A1
Chronic enteropathy associated with SLCO2A1 gene
Chinese
الوصول للمادة أونلاين:https://doi.org/10.1186/s13023-024-03177-y

الانترنت

https://doi.org/10.1186/s13023-024-03177-y

مواد مشابهة