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                                       Details for article 2 of 50 found articles
 
 
  A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII)
 
 
Title: A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII)
Author: Huie, M. L.
Chen, A. S.
Brooks, S.Sklower
Grix, A.
Hlrschhorn, R.
Appeared in: Human molecular genetics
Paging: Volume 3 (1994) nr. 7 pages 1081-1087
Year: 1994-07
Contents:
Publisher: Oxford University Press, Oxford
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 2 of 50 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands