טוען...
Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests
An individual with familial dysalbuminemic hyperthyroxinemia (FDH) due to a homozygous mutation (c.653G>A, p.R218H) in the human serum albumin (HSA) gene is reported. The patient was identified during evaluation of abnormal thyroid tests in a large family with multiple levels of consanguinity. He...
שמור ב:
| הוצא לאור ב: | Thyroid |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Mary Ann Liebert, Inc.
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5994679/ https://ncbi.nlm.nih.gov/pubmed/29676214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2017.0564 |
| תגים: |
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