SCOPUS 정보 검색 플랫폼

Volumn 28, Issue 1, 1997, Pages 12-14

Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein

(12) Mitchison, Hannah M a Taschner, P E M b Kremmidiotis, C c Callen, D F c Doggett, N A d Lerner, T J e Janes, R B f Wallace, B A f Munroe, Patricia B a O'Rawe, Angela M a Gardiner, R M a Mole, Sara E a

a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL (United Kingdom)

b LEIDEN UNIVERSITY (Netherlands)

c WOMEN S AND CHILDREN S HOSPITAL (Australia)

d LOS ALAMOS NATIONAL LABORATORY (United States)

e MASSACHUSETTS GENERAL HOSPITAL (United States)

f UNIVERSITY OF LONDON (United Kingdom)

Author keywords

CLN3 gene; Juvenile NCL; Protein

Indexed keywords

PROTEIN;

ARTICLE; FUNGAL GENETICS; GENE SEQUENCE; GENE STRUCTURE; HUMAN; NEURONAL CEROID LIPOFUSCINOSIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SACCHAROMYCES CEREVISIAE; SEQUENCE HOMOLOGY;

EID: 8544241735 PISSN: 0174304X EISSN: None Source Type: Journal
DOI: 10.1055/s-2007-973656 Document Type: Article

Times cited : (19)

References (5)

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- Identifying nonpolar transbilayer helices in amino acid sequences of membrane proteins
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3
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- YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2
- Järvelä, I. E , H. M. Mitchison, A. M. O'Rawe, P. B. Munroe, P. E. M. Taschner, N. de Vos, T. J. Lerner, K. L. D'Arigo, D. F. Callen, A. D. Thompson, M. Knight, B. L. Marrone, M O. Mundt, L. Meincke, M. H. Breuning, R. M. Gardiner, N. A. Doggett, S. E. Mole: YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2. Genomics 29 (1995) 478-489
- (1995) Genomics , vol.29 , pp. 478-489
- Järvelä, I.E.¹ Mitchison, H.M.² O'Rawe, A.M.³ Munroe, P.B.⁴ Taschner, P.E.M.⁵ De Vos, N.⁶ Lerner, T.J.⁷ D'Arigo, K.L.⁸ Callen, D.F.⁹ Thompson, A.D.¹⁰ Knight, M.¹¹ Marrone, B.L.¹² Mundt, M.O.¹³ Meincke, L.¹⁴ Breuning, M.H.¹⁵ Gardiner, R.M.¹⁶ Doggett, N.A.¹⁷ Mole, S.E.¹⁸

4
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- Strategy for mutation detection in CLN3 Characterisation of two Finnish mutations
- Munroe, P. B., A. M. O'Rawe, H. M. Mitchison, I. E. Järvelä, P. Santavuouri, T. J. Lerner, P. E. M. Taschner, R. M. Gardiner, S. E Mole: Strategy for mutation detection in CLN3 Characterisation of two Finnish mutations. Neuropediatrics 28 (1997) 15-17
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- Munroe, P.B.¹ O'Rawe, A.M.² Mitchison, H.M.³ Järvelä, I.E.⁴ Santavuouri, P.⁵ Lerner, T.J.⁶ Taschner, P.E.M.⁷ Gardiner, R.M.⁸ Mole, S.E.⁹

5
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- Isolation of a novel gene underlying Batten disease (CLN3)
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