Breaking the rule of three

Nature

Volumn 386, Issue 6627, 1997, Pages 767-769

  Mandel, Jean Louis ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE CLASSIFICATION; EPILEPSY; FRAGILE X SYNDROME; GENETIC DISORDER; GENETIC STABILITY; HUMAN; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SHORT SURVEY; GENETICS; MYOCLONUS EPILEPSY; NOTE; TRINUCLEOTIDE REPEAT;

CYSTATIN; CYSTATIN B;

CYSTATINS; EPILEPSIES, MYOCLONIC; GENETIC DISEASES, INBORN; HUMANS; REPETITIVE SEQUENCES, NUCLEIC ACID; TRINUCLEOTIDE REPEATS;

EID: 0031585131     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/386767a0     Document Type: Short Survey

References (12)

1. Paulson, H. L. & Fischbeck, K. H. Annu. Rev. Neurosci. 19, 79-107 (1996).
2. Lalioti, M. D. et al. Nature 386, 847-851 (1997).
3. Lafrenière, R. G. et al. Nature Genet. 15, 298-302 (1997).
4. Virtaneva, K. et al. Nature Genet. 15, 393-396 (1997).
5. Wells, R. D. J. Biol. Chem. 271, 2875-2878 (1996).
6. Campuzano, V. et al. Science 271, 1423-1427 (1996).
7. Cossée, M. et al. Proc. Natl Acad. Sci. USA (in the press).
8. Pennacchio, L. A. et al. Science 271, 1731-1734 (1996).
9. Buard, J. & Jeffreys, A. J. Nature Genet. 15, 327-328 (1997).
10. Yu, S. et al. Cell 88, 367-374 (1997).
11. Knebelmann, B. et al. Am. J. Hum. Genet. 59, 1221-1232 (1996).
12. Schiaffino, M. V. et al. Hum. Mol. Genet. 4, 2319-2325 (1995).