The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia-Reference-Cited by-同舟云学术

The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Published:1992-08-07 Issue:5071 Volume:257 Page:797-800
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Koch Manuela C.¹,Steinmeyer Klaus²,Lorenz Claudius²,Ricker Kenneth³,Wolf Friedrich¹,Otto Michael¹,Zoll Barbara⁴,Lehmann-Horn Frank⁵,Grzeschik Karl-Heinz¹,Jentsch Thomas J.²

Affiliation:

1. Medical Center for Human Genetics, Marburg University, D-3550 Marburg, Germany.

2. Center for Molecular Neurobiology (ZMNH), Hamburg University, D-2000 Hamburg 20, Germany.

3. Clinical Neurology, Würzburg University, D-8700 Würzburg, Germany.

4. Institute for Human Genetics, Göttingen University, D-3400 Göttingen, Germany.

5. Clinical Neurology, Technical University, D-8000 Munich, Germany.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference25 articles.

1. BAUER, C.K., COMPLETELY FUNCTIONAL DOUBLE-BARRELED CHLORIDE CHANNEL EXPRESSED FROM A SINGLE TORPEDO CDNA, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 88: 11052 (1991).

2. Myotonia Congenita and Syndromes Associated with Myotonia 1977

3. BRETAG, A.H., MUSCLE CHLORIDE CHANNELS, PHYSIOLOGICAL REVIEWS 67: 618 (1987).

4. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

5. EIBERG, H, GENETICS AND LINKAGE RELATIONSHIPS OF THE C-3 POLYMORPHISM - DISCOVERY OF C3-SE LINKAGE AND ASSIGNMENT OF LES-C3-DM-SE-PEPD-LU SYNTENY TO CHROMOSOME-19, CLINICAL GENETICS 24: 159 (1983).

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