Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)-Reference-Cited by-同舟云学术

Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)

Published:1996-03-22 Issue:5256 Volume:271 Page:1731-1734
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Pennacchio Len A.¹,Lehesjoki Anna-Elina²,Stone Nancy E.³,Willour Virginia L.³,Virtaneva Kimmo²,Miao Jinmin²,D'Amato Elena²,Ramirez Lucia³,Faham Malek³,Koskiniemi Marjaleena⁴,Warrington Janet A.³,Norio Reijo⁵,de la Chapelle Albert²,Cox David R.³,Myers Richard M.³

Affiliation:

1. L. A. Pennacchio, Department of Genetics, Stanford University School of Medicine, and Department of Biology, Stanford University, Stanford, CA 94305, USA.

2. A.-E. Lehesjoki, K. Virtaneva, J. Miao, E. D'Amato, A. de la Chapelle, Department of Medical Genetics, University of Helsinki, Haartmaninkatu 3, 00290 Helsinki, Finland.

3. N. E. Stone, V. L. Willour, L. Ramirez, M. Faham, J. A. Warrington, D. R. Cox, R. M. Myers, Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.

4. M. Koskiniemi, Department of Virology, University of Helsinki, Haartmaninkatu 3, 00290 Helsinki, Finland.

5. R. Norio, Department of Medical Genetics, Finnish Population and Family Welfare Federation, 00100 Helsinki, Finland.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference35 articles.

1. THE HUMAN CYSTATIN-C GENE (CST3), MUTATED IN HEREDITARY CYSTATIN-C AMYLOID ANGIOPATHY, IS LOCATED ON CHROMOSOME-20;ABRAHAMSON M;HUMAN GENETICS,1989

2. PROGRESSIVE MYOCLONUS EPILEPSIES - SPECIFIC CAUSES AND DIAGNOSIS;BERKOVIC F. S.;NEW ENGLAND JOURNAL OF MEDICINE,1986

3. ORGANIZATION AND EXPRESSION OF EUKARYOTIC SPLIT GENES-CODING FOR PROTEINS;BREATHNACH R;ANNUAL REVIEW OF BIOCHEMISTRY,1981

4. BALTIC MYOCLONUS EPILEPSY - HEREDITARY DISORDER OF CHILDHOOD MADE WORSE BY PHENYTOIN;ELDRIDGE R;LANCET,1983

5. FAHAM M unpublished data.

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