Difference between revisions of "FH"
(Created page with "==Annotation== ===Name=== FH ===Alias=== FUMH_HUMAN ===Disease=== Disease: Fumarase deficiency [http://www.ncbi.nlm.nih.gov/pubmed/9635293 (PMID:9635293)] Dysfunction type:...") |
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Latest revision as of 01:52, 5 November 2018
Contents
Annotation
Name
FH
Alias
FUMH_HUMAN
Disease
Disease: Fumarase deficiency (PMID:9635293)
Dysfunction type: NA
Description: Fumarase deficiency is caused by mutations affecting the FH.
Function
Function Mechanism: NA (PMID:9635293)
Biological Process: pathogenic process
Description: snp in lncRNA
