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  • Molecular Mechanisms of Ataxia Telangiectasiaby Shamim I. Ahmad

    Landes Bioscience 2009; US$ 129.00

    Ataxia telangiectasia (AT) is an incurable, rare autosomal recessive genetic disorder which affects approximately one in 40,000-100,000 and the carrier frequency is estimated to be 1:100-200. In the United Kingdom it affects 1 in 300,000 live births amounting to about 5 or 6 cases per year. Although the medial survival rate of affected persons is between... more...

  • Molecular Mechanisms of Cockayne Syndromeby Shamim I. Ahmad

    Landes Bioscience 2009; US$ 129.00

    Cockayne syndrome (CS) is a rare autosomal genetic disorder that was first identified almost 62 years ago by Alfred Cockayne and was named after him. The earliest publication record (PubMed) available is a paper by Marie et al in 1958. Since then 815 research papers including excellent reviews have been published (PubMed, December 2008), yet we are... more...

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