MeSH Browser

MeSH Supplementary: Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria
Unique ID: C565499
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565499
Registry Numbers: 0
Heading Mapped to: *Intellectual Disability; *Hyperlysinemias
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria MeSH Supplementary Concept Data 2025