HOMOZYGOSITY FOR THE F119L MUTATION IN THE PMM2 GENE IN AN ADULT WITHCDG SYNDROME TYPE IA

Authors
VANTINTELEN P MATTHIJS G BRAAM W CASSIMAN JJ DURAN M POLLTHE BT
Citation
P. Vantintelen et al., HOMOZYGOSITY FOR THE F119L MUTATION IN THE PMM2 GENE IN AN ADULT WITHCDG SYNDROME TYPE IA, European journal of human genetics, 6, 1998, pp. 1097-1097
Citations number
NO
Categorie Soggetti
Genetics & Heredity",Biology
Journal title
European journal of human genetics → ACNP
ISSN journal
10184813
Volume
6
Year of publication
1998
Supplement
1
Pages
1097 - 1097
Database
ISI
SICI code
1018-4813(1998)6:<1097:HFTFMI>2.0.ZU;2-7