http://www.cnr.it/ontology/cnr/individuo/prodotto/ID109976
Two new mutations causing an amino acid substitution in the H helix of the alpha chain: differential metabolic mRNA patterns underlying the alpha thalassemia phenotype and the absence of the Hb variants in the erithocytes. (Comunicazione a convegno)
- Type
- Label
- Two new mutations causing an amino acid substitution in the H helix of the alpha chain: differential metabolic mRNA patterns underlying the alpha thalassemia phenotype and the absence of the Hb variants in the erithocytes. (Comunicazione a convegno) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
- Alternative label
Lacerra G., Musollino G., Di Noce F., Gaudiano C., Masciandaro S., Mercedes C., Amato R., Miraglia E., Friscia M.G., Ciaccio C., Virruso L., Di Girgenti C., Lagona L., Medulla E., Carestia C. (2003)
Two new mutations causing an amino acid substitution in the H helix of the alpha chain: differential metabolic mRNA patterns underlying the alpha thalassemia phenotype and the absence of the Hb variants in the erithocytes.
in 9th International conference on Thalassaemia and the Haemoglobinopathies, Città del Mare, Terrasini (PA)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Lacerra G., Musollino G., Di Noce F., Gaudiano C., Masciandaro S., Mercedes C., Amato R., Miraglia E., Friscia M.G., Ciaccio C., Virruso L., Di Girgenti C., Lagona L., Medulla E., Carestia C. (literal)
- Titolo
- Two new mutations causing an amino acid substitution in the H helix of the alpha chain: differential metabolic mRNA patterns underlying the alpha thalassemia phenotype and the absence of the Hb variants in the erithocytes. (literal)
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- Autore CNR
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