Search Results - Shadrina, Marya I.

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  1. 1
    A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia

    A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia by Slominsky, Petr A., Markova, Elena D., Shadrina, Marya I., Illarioshkin, Sergey N., Miklina, Natalia I., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A.

    Published in Human mutation
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    CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C

    CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C by Slominsky, Petr A., Shadrina, Marya I., Kondratyeva, Ekaterina A., Tupitsina, Tatiana V., Levitsky, Gleb N., Skvortsova, Veronika I., Limborska, Svetlana A.

    Published in Human mutation
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  3. 3
    A common 3-bp deletion in theDYT1 gene in Russian families with early-onset torsion dystonia

    A common 3-bp deletion in theDYT1 gene in Russian families with early-onset torsion dystonia by Slominsky, Petr A., Markova, Elena D., Shadrina, Marya I., Illarioshkin, Sergey N., Miklina, Natalia I., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A.

    Published in Human mutation
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