Cite
HARVARD Citation
Amir, R. et al. (2005). Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. Journal of medical genetics. 42 (2), p. e15. [Online].
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Amir, R. et al. (2005). Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. Journal of medical genetics. 42 (2), p. e15. [Online].