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hemoglobin Görwihl

has the mutation (alpha2beta(2)5(A2)Pro to Ala), an electrophoretically silent variant with impaired glycation

Also Known As:

Hb Görwihl

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Blood Proteins: 12459
    - Hemoglobins: 37188
      - Abnormal Hemoglobins: 120
        hemoglobin Görwihl: 1
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        hemoglobin Görwihl: 1

Experts

1.	Cannata, Monica: 1 article (04/2015)
2.	Cassarà, Filippo: 1 article (04/2015)
3.	Giambona, Antonino: 1 article (04/2015)
4.	Leto, Filippo: 1 article (04/2015)
5.	Maggio, Aurelio: 1 article (04/2015)
6.	Passarello, Cristina: 1 article (04/2015)
7.	Vinciguerra, Margherita: 1 article (04/2015)

Related Diseases

1.

04/01/2015 - "This work allowed us to describe the co-inheritance of three rare β hemoglobin variants with other alterations in globin genes: the β hemoglobin variant Hb Yaounde [β134(H12)Val>Ala], found for the first time in combination with ααα(anti3.7) arrangement, and the β hemoglobin variants Hb Görwihl [β5(A2)Pro>Ala] and Hb City of Hope [β69(E13)Gly>Ser], found both in association with β(0) -thalassemia. "

Related Drugs and Biologics

1.	Hemoglobins (Hemoglobin)
2.	Globins
3.	hemoglobin Yaounde
4.	hemoglobin City of Hope