Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease-Reference-Cited by-同舟云学术

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Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

Published:1993-12-24 Issue:5142 Volume:262 Page:2039-2042
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Bergoffen J.¹,Scherer S. S.²,Wang S.²,Scott M. Oronzi²,Bone L. J.²,Paul D. L.³,Chen K.²,Lensch M. W.²,Chance P. F.²⁴,Fischbeck K. H.²

Affiliation:

1. Pennsylvania Medical School and Genetics Division, Children's Hospital of Philadelphia, Philadelphia, PA 19104.

2. Department of Neurology, University of Pennsylvania Medical School, Philadelphia, PA 19104.

3. Department of Neurobiology, Harvard Medical School, Boston, MA 02115.

4. Neurology Division, Children's Hospital of Philadelphia, Philadelphia, PA 19104.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference30 articles.

1. AKERT, K, FINE-STRUCTURE OF PERINEURAL ENDOTHELIUM, CELL AND TISSUE RESEARCH 165: 281 (1976).

2. BECKETT, J, LOCALIZATION OF X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE (CMT 2) TO XQ13, JOURNAL OF NEUROGENETICS 3: 225 (1986).

3. BELLIVEAU, D.J., EXPRESSION OF GAP JUNCTION GENES DURING POSTNATAL NEURAL DEVELOPMENT, DEVELOPMENTAL GENETICS 12: 308 (1991).

4. BENNETT, MVL, GAP-JUNCTIONS - NEW TOOLS, NEW ANSWERS, NEW QUESTIONS, NEURON 6: 305 (1991).

5. BERGOFFEN, J, LINKAGE LOCALIZATION OF X-LINKED CHARCOT-MARIE-TOOTH DISEASE, AMERICAN JOURNAL OF HUMAN GENETICS 52: 312 (1993).

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