Author:
Li Mei-rong,Pan Hong,Bao Xin-Hua,Zhang Yu-Zhi,Wu Xi-Ru
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference38 articles.
1. Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JM (1992) Methylation of HpaII and HhaII sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51:1229–1239
2. Amano K, Nomura Y, Segawa M, Yamakawa K (2000) Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome. J Hum Genet 45:231–236
3. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999) Rett syndrome is caused by mutation in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23:185–188
4. Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB (2005) Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. J Med Genet 42:e15
5. Archer HL, Evans JC, Edwards S, Colley J, Newbury-Ecob R, O’callaghan F, Huyton M, O’Regan M, Tolmie J, Sampson J, Clarke AJ, Osborne J (2006a) CDKL5 mutations cause infantile spasms, early onset seizures and severe mental retardation in female patients. J Med Genet 12 Apr (published online)
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