The molecular-genetic basis of atransferrinemia

 
English | Català | Español
 

The molecular-genetic basis of atransferrinemia has been previously determined in only 3 human instances. As long as it may be relevant in establishing the etiology of a clinically severe form of atransferrinemia, here we report the Molecular-genetic characterization of Violet’s atransferrinemia case .

Other published molecular-genetic characterizations are:

Molecular-genetic characterization of slovakian girl
Molecular-genetic characterization of a american woman

Molecular-genetic characterization of an italian boy

We are acknowledged and thankful to MD Ernest Beutler for his findings in Violet’s Case


Home