Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 1, 2016Japanese Clinical MedicineOpen Access

Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P)

View Full Paper
Ask AI
Bookmark
Share

Authors

YOYoshinori OsakiYHYoshitaka HayashiYNYoshinori Nakagawa

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Osaki et al. (2016) studied this question.

synapsesocial.com/papers/6a96faa52d8f86faeeb2fff1https://doi.org/10.4137/jcm.s38990
View Full Paper
Ask AI
Bookmark
Share