✦ LIBER ✦

Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in theNYXgene

✍ Scribed by Felix K. Jacobi, Sten Andréasson, Hana Langrova, Alfons Meindl, Eberhart Zrenner, Eckart Apfelstedt-Sylla, Carsten M. Pusch

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A phenotypic study of congenital station

✍ Panagiotis I. Sergouniotis; Anthony G. Robson; Zheng Li; Sophie Devery; Graham E 📂 Article 📅 2011 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 272 KB

A novel CACNA1F mutation in a french fam

✍ Felix Karl Jacobi; Christian P. Hamel; Bernard Arnaud; Nikolaus Blin; Martina Br 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 191 KB

The complete form of X-linked congenital

✍ Meindl, Alfons; Pusch, Carsten M.; Zeitz, Christina; Brandau, Oliver; Pesch, Kat 📂 Article 📅 2000 🏛 Nature Publishing Group 🌐 English ⚖ 504 KB

Abnormalities of the scotopic threshold

✍ Keith Bradshaw; Douglas Newman; Louise Allen; Anthony Moore 📂 Article 📅 2003 🏛 Springer-Verlag 🌐 English ⚖ 555 KB

Development of a 1.4-Mb BAC/PAC Contig a

✍ R.L. Sparkes; C.G. Summer; K.M. Boycott; R.J. Zahorchak; N.T. Bech-Hansen 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 62 KB