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About this Biochemistry, Genetics and Molecular Biology article

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes by Sonia Nouioua; Tarik Hamadouche; Benoit Funalot; Rafaëlle Bernard; Nora Bellatache; Radia Bouderba; Djamel Grid; Salima Assami; Traki Benhassine; Nicolas Levy; Jean-Michel Vallat; Meriem Tazir is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Sonia Nouioua; Tarik Hamadouche; Benoit Funalot; Rafaëlle Bernard; Nora Bellatache; Radia Bouderba; Djamel Grid; Salima Assami; Traki Benhassine; Nicolas Levy; Jean-Michel Vallat; Meriem Tazir
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
Published
2011
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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Browse all works by Sonia Nouioua; Tarik Hamadouche; Benoit Funalot; Rafaëlle Bernard; Nora Bellatache; Radia Bouderba; Djamel Grid; Salima Assami; Traki Benhassine; Nicolas Levy; Jean-Michel Vallat; Meriem Tazir