Novel solute carrier family 26, member 3 mutation in a prenatal recurrent case with congenital chloride diarrhea-Reference-Cited by-同舟云学术

Novel solute carrier family 26, member 3 mutation in a prenatal recurrent case with congenital chloride diarrhea

Author:

Wu Siqi¹²,Han Jin¹²³^ORCID,Zhang Yongling³,Ye Zhichao¹,Lu Ping¹,Tian Kege¹

Affiliation:

1. Department of Prenatal DiagnosisDongguan Kanghua Hospital Dongguan China

2. Department of Obstetrics and GynecologyGuangzhou Medical University Guangzhou China

3. Department of Prenatal diagnosisGuangzhou Women and Children's Medical Center Guangzhou China

Funder

The Science and Technology Program of Dongguan

The Science and Technology Program of Guangdong

The Science and Technology Program of Guangzhou

Publisher

Wiley

Subject

Obstetrics and Gynecology

Link

Reference15 articles.

2. Familial chloride diarrhoea (congenital alkalosis with diarrhoea);Davidson AG;Aust Paediatr J,1972

5. Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea;Moseley RH;Am J Physiol,1999

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