MeSH Browser

MeSH Supplementary: hemoglobin Barika
Unique ID: C519336
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C519336
Entry Term(s): Hb Barika
Registry Numbers: 0
Heading Mapped to: *Hemoglobins, Abnormal
Frequency: 1
Note: has mutation alpha42(C7)Tyr to His (alpha2) which leads to an alpha+ -Thalassemia-like syndrome
Source: Hemoglobin 2007;31(1):17-22
Date of Entry: 2007/05/03
Revision Date: 1955/01/01

hemoglobin Barika MeSH Supplementary Concept Data 2025