Skip to Main Content
Advertisement
Close
ASH Clinical News
ASH News Daily
ASH-SAP
Blood
Blood Advances
Hematology
The Hematologist
International
Blood Chinese Edition
Blood Japanese Edition
Blood Italian Edition
Blood Latin America Edition
Blood Spanish Edition
ASH
ASH Home
Research
Education
Advocacy
Meetings
Publications
ASH Store
Cart
User Tools Dropdown
Cart
Sign In
Search Dropdown Menu
header search
search input
Search input auto suggest
filter your search
All Content
All Journals
Blood
Search
Toggle Menu
Menu
Issues
Current Issue
All Issues
First edition
Abstracts
2022 Annual Meeting
2022 Late Breaking
2021 Annual Meeting
2020 Annual Meeting
2020 Late Breaking
2019 Annual Meeting
2019 Late Breaking
All Meeting Abstracts
Collections
Collections
Special Collections
Multimedia
Alerts
Author Center
Submit
Author Guide
Style Guide
Why Submit to Blood?
About
About Blood
Editorial Board and Staff
Subscriptions
Public Access
Copyright
Alerts
Blood Classifieds
Skip Nav Destination
A point mutation in the coding region of uroporphyrinogen decarboxylase associated with familial porphyria cutanea tarda
Blood
(1989) 73 (4): 892–895.
Currently there are no citedby results. Try again later.
Close Modal
Close Modal
This Feature Is Available To Subscribers Only
Sign In
or
Create an Account
Close Modal
Close Modal
Advertisement
close advertisement
