Novel compound heterozygote mutations of TJP2 in a Chinese child with progressive cholestatic liver disease.

Novel compound heterozygote mutations of TJP2 in a Chinese child with progressive cholestatic liver disease. — المؤلف: Ge, Ting — BMC medical genetics 20190820

المؤلف
Ge, Ting
النشر
BMC medical genetics 20190820
الوصف
18 p.
الموضوعات
China؛ Cholestasis, Intrahepatic؛ Female؛ Heterozygote؛ High-Throughput Nucleotide Sequencing؛ Humans؛ Infant؛ Maternal Inheritance