Skip to content

Opening book details…

About this Biochemistry, Genetics and Molecular Biology article

A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot–Marie–Tooth disease with irregularly folded myelin sheaths by Eva Nelis; Sevim Erdem; Ersin Tan; Ann Löfgren; Chantal Ceuterick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman; Haluk Topaloglu 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
Eva Nelis; Sevim Erdem; Ersin Tan; Ann Löfgren; Chantal Ceuterick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman; Haluk Topaloglu
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
Published
2002
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

More by Eva Nelis; Sevim Erdem; Ersin Tan; Ann Löfgren; Chantal Ceuterick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman; Haluk Topaloglu

Browse all works by Eva Nelis; Sevim Erdem; Ersin Tan; Ann Löfgren; Chantal Ceuterick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman; Haluk Topaloglu