A bill to amend the Public Health Service Act to improve the diagnosis and treatment of hereditary hemorrhagic telangiectasia, and for other purposes.
The bill’s titles are written by its sponsor.
Sponsor. Senator for South Dakota. Democrat.
Last Updated: May 8, 2013
Length: 16 pages
May 8, 2013
113th Congress, 2013–2015
Died in a previous Congress
This bill was introduced on May 8, 2013, in a previous session of Congress, but was not enacted.
Jun 9, 2011
Earlier Version — Introduced
This activity took place on a related bill, S. 1167 (112th).
May 8, 2013
Bills and resolutions are referred to committees which debate the bill before possibly sending it on to the whole chamber.
S. 908 (113th) was a bill in the United States Congress.
A bill must be passed by both the House and Senate in identical form and then be signed by the President to become law.
This bill was introduced in the 113th Congress, which met from Jan 3, 2013 to Jan 2, 2015. Legislation not enacted by the end of a Congress is cleared from the books.
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Civic Impulse. (2017). S. 908 — 113th Congress: Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2013. Retrieved from https://www.govtrack.us/congress/bills/113/s908
“S. 908 — 113th Congress: Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2013.” www.GovTrack.us. 2013. November 20, 2017 <https://www.govtrack.us/congress/bills/113/s908>
|title=S. 908 (113th)
|accessdate=November 20, 2017
|author=113th Congress (2013)
|date=May 8, 2013
|quote=Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2013
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