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About this Biochemistry, Genetics and Molecular Biology article

C.O.1 Identification of a new gene mutated in autosomal recessive centronuclear myopathy, and functional links with the dominant form by A. Nicot; A. Toussaint; V. Tosch; C. Kretz; C. Wallgren-Pettersson; E. Iwarsson; H. Kingston; J. Garnier; V. Biancalana; J. Mandel; J. Laporte 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
A. Nicot; A. Toussaint; V. Tosch; C. Kretz; C. Wallgren-Pettersson; E. Iwarsson; H. Kingston; J. Garnier; V. Biancalana; J. Mandel; J. Laporte
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
Published
2007
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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Browse all works by A. Nicot; A. Toussaint; V. Tosch; C. Kretz; C. Wallgren-Pettersson; E. Iwarsson; H. Kingston; J. Garnier; V. Biancalana; J. Mandel; J. Laporte