About this Biochemistry, Genetics and Molecular Biology article
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans. by Wilkes, D; Rutland, P; Pulleyn, L J; Reardon, W; Moss, C; Ellis, J P; Winter, R M; Malcolm, S is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
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- Author
- Wilkes, D; Rutland, P; Pulleyn, L J; Reardon, W; Moss, C; Ellis, J P; Winter, R M; Malcolm, S
- Publisher
- BMJ Publishing Group; BMJ (ISSN 0022-2593)
- Published
- 1996
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)