Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.

Name: Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.
Author: Zhou, Haiyang

Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review. — المؤلف: Zhou, Haiyang — BMC endocrine disorders 20190222

المؤلف: Zhou, Haiyang
النشر: BMC endocrine disorders 20190222
الوصف: 82 p.
الموضوعات: Gitelman Syndrome؛ Graves Disease؛ Homozygote؛ Humans؛ Male؛ Middle Aged؛ Mutation؛ Solute Carrier Family 12, Member 3