✦ LIBER ✦

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

✍ Scribed by Evans, Julie C; Archer, Hayley L; Whatley, Sharon D; Kerr, Alison; Clarke, Angus; Butler, Rachel

Book ID: 110025675
Publisher: Nature Publishing Group
Year: 2004
Tongue: English
Weight: 109 KB
Volume: 13
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5201270

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Variation in novel exons (RACEfrags) of

Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls

✍ Periklis Makrythanasis; Philipp Kapranov; Lucia Bartoloni; Alexandre Reymond; Sa 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 586 KB

The study of transcription using genomic tiling arrays has lead to the identification of numerous additional exons. One example is the MECP2 gene on the X chromosome; using 5'RACE and RT-PCR in human tissues and cell lines, we have found more than 70 novel exons (RACEfrags) connecting to at least on

Deleterious mutations in exon 1 of MECP2

Deleterious mutations in exon 1 of MECP2 in Rett syndrome

✍ Aline Quenard; Saliha Yilmaz; Hervé Fontaine; Thierry Bienvenu; Anne Moncla; Vin 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 484 KB

Mutations found within exon 1 of MECP2 i

Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome

📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 131 KB

Novel exon 1 mutations in MECP2 implicat

Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome

✍ Carol J. Saunders; Berge E. Minassian; Eva W.C. Chow; Weiwei Zhao; John B. Vince 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 92 KB 👁 2 views

No mutations in the coding region of the

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients

✍ Vourc'h, Patrick; Bienvenu, Thierry; Beldjord, Cherif; Chelly, Jamel; Barthélémy 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 74 KB

Discovery of a new protein isoform of Me

Discovery of a new protein isoform of MeCP2 and exon 1 mutations causing Rett syndrome

✍ Simon Warby 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 786 KB