Electronic Resource
[s.l.]
:
Nature Publishing Group
Nature
356 (1992), S. 15-15
ISSN:
1476-4687
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
Notes:
[Auszug] THE identification over the past year of the mutations involved in three neurological disorders - fragile X syndrome1' 3, spinal bulbar muscular atrophy4 and, now, myotonic dystrophy5"10 - has revealed that a common genetic mechanism underlies them all. This creates a very exciting prospect: the ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/356015a0
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