✦ LIBER ✦

The Location of HumanCASKat Xp11.4 Identifies This Gene as a Candidate for X-Linked Optic Atrophy

✍ Scribed by Spiros D. Dimitratos; Dean G. Stathakis; Carrie A. Nelson; Daniel F. Woods; Peter J. Bryant

Book ID: 115614397
Publisher: Elsevier Science
Year: 1998
Tongue: English
Weight: 56 KB
Volume: 51
Category: Article
ISSN: 0888-7543
DOI: 10.1006/geno.1998.5404

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Gene for X-Linked Optic Atrophy Is Clo

A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

✍ Jacqueline J.M. Assink; Nel T. Tijmes; Jacoline B. ten Brink; Roelof-Jan Oostra; 📂 Article 📅 1997 🏛 American Society of Human Genetics 🌐 English ⚖ 103 KB

The CASK gene harbored in a deletion det

The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation

✍ Shin Hayashi; Seiji Mizuno; Ohsuke Migita; Torayuki Okuyama; Yoshio Makita; Akir 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB 👁 2 views

Detection of a new polymorphism in the p

Detection of a new polymorphism in the plasma-membrane Ca2+ATPase isoform-3 gene and its exclusion as a candidate for X-linked myotubular myopathy (MTM1)

✍ Z. Smolenicka; D. Guerini; E. Carafoli; W. Kress; S. Liechti-Gallati 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 102 KB