✦ LIBER ✦

Complete genomic structure of the CLCN6 and CLCN7 putative chloride channel genes

✍ Scribed by Uwe Kornak; Michael R. Bösl; Christian Kubisch

Book ID: 114148578
Publisher: Elsevier Science
Year: 1999
Tongue: English
Weight: 432 KB
Volume: 1447
Category: Article
ISSN: 0167-4781
DOI: 10.1016/s0167-4781(99)00128-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The human and mouse methylenetetrahydrof

The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene

✍ Derval J. Gaughan; Sandrine Barbaux; Leo A.J. Kluijtmans; Alexander S. Whitehead 📂 Article 📅 2000 🏛 Elsevier Science 🌐 English ⚖ 454 KB

Cloning and Characterization of CLCN5, t

Cloning and Characterization of CLCN5, the Human Kidney Chloride Channel Gene Implicated in Dent Disease (an X-Linked Hereditary Nephrolithiasis)

✍ SIMON E. FISHER; INGE VANBAKEL; SARAH E. LLOYD; SIMON H.S. PEARCE; RAJESH V. THA 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 374 KB

G.P.99 Molecular genetic diagnostics of

G.P.99 Molecular genetic diagnostics of myotonia congenita and analysis of the effects of mutations in the CLCN1 gene on the structure of the dimeric ClC1 chloride channel

✍ Fajkusova, L.; Zı´dková, J.; Paclová, D.; Marek, J.; Voháòka, S.; Hermanová, M. 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 49 KB

Assignment of the Genes Encoding the Hum

Assignment of the Genes Encoding the Human Chloride Channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32–q33 byin SituHybridization

✍ Fumiko Saito-Ohara; Shinichi Uchida; Yasuo Takeuchi; Sei Sasaki; Aiko Hayashi; F 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 202 KB

Identification of five new mutations and

Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita

✍ F Sangiuolo; A Botta; A Mesoraca; S Servidei; L Merlini; G Fratta; G Novelli; B 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 143 KB 👁 2 views

Autosomal dominant myotonia congenita or Thomsen's disease (OMIM\* 160800) and autosomal recessive myotonia congenita or Becker's (OMIM\* 255700) are rare nondystrophic disorders due to allelic mutations of the muscle chloride channel gene, CLCN1. We have analysed all 24 exons of the CLCN1 gene, in

Refined Genomic Localization of the Gene

Refined Genomic Localization of the Genetic Lesion in theOsteopetrosis(op) Rat and Exclusion of Three Positional and Functional Candidate Genes,Clcn7, Atp6v0c, andSlc9a3r2

✍ B. Perdu; P. R. Odgren; L. Van Wesenbeeck; K. Jennes; C. C. MacKay; W. Van Hul 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 237 KB