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A new mutation c.422C>G (p.S141C) in homoand heterozygous forms of the human leptin gene

✍ Scribed by M. K. Chekhranova; S. K. Karpova; S. B. Yatsyshina; J. A. Pankov

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A new compound heterozygous for c.886C>T

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Identification of mutation c.632G>A (p.G

✍ Feng-Yan Lu; Ling Xu; Xun-Guo Yin; Ping Wan; Xiao-De Zhang; Wei-Wen Chen; Shao-P 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 310 KB

Association of a missense mutation in th

✍ Fiona C Buchanan; Carolyn J Fitzsimmons; Andrew G Van Kessel; Tracey D Thue; Dia 📂 Article 📅 2002 🏛 BioMed Central 🌐 French ⚖ 730 KB

Pyrimidine-5′-nucleotidase Campinas, a n

✍ dos Santos, Andrey; Dantas, Larissa Elizabeth Cordeiro; Traina, Fabiola; de Albu 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 975 KB

Identification of a new splicing mutatio

✍ A. Bonizzato; E. Nicolis; P. Gasparini 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 154 KB 👁 1 views

Cystic fibrosis (CF) is one of the most common severe autosomal recessive disease in Caucasians,

Haemophilia B caused by a point mutation

✍ Rees, D. J. G.; Rizza, C. R.; Brownlee, G. G. 📂 Article 📅 1985 🏛 Nature Publishing Group 🌐 English ⚖ 456 KB