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C.P.2.12 Congenital muscular dystrophy with mental retardation, dilated cardiomyopathy and abnormally located mitochondria

✍ Scribed by B. Talim; B. Koksal; Z. Akcoren; M. Topcu; D. Alehan; G. Kale; H. Topaloglu

No coin nor oath required. For personal study only.

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POMT2 intragenic deletions and splicing

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C.P.3.03 Novel POMT2 mutations associate

✍ A. Yanagisawa; C. Bouchet; H. Manya; S. Quijano-Roy; P. van den Bergh; L. Violle 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 50 KB