AI Assistant
Blog
Pricing
Log In
Sign Up
Homozygous missense variant of PTH (c.166C>T, p.(Arg56Cys)) as the cause of familial isolated hypoparathyroidism in a three-year-old child
Details
Cite
Export
Add to List
The content you want to view is only available to
Zendy Plus
users.
Already have an account? Click
here.
to sign in.
