THE LONG-TERM EVOLUTION OF A CASE OF 3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A LYASE DEFICIENCY ASSOCIATED WITH DEAFNESS AND RETINITIS-PIGMENTOSA

Authors
JONES KJ WILCKEN B KILHAM H
Citation
Kj. Jones et al., THE LONG-TERM EVOLUTION OF A CASE OF 3-HYDROXY-3-METHYLGLUTARYL-COENZYME-A LYASE DEFICIENCY ASSOCIATED WITH DEAFNESS AND RETINITIS-PIGMENTOSA, Journal of inherited metabolic disease, 20(6), 1997, pp. 833-834
Citations number
2
Categorie Soggetti
Endocrynology & Metabolism","Genetics & Heredity
Journal title
Journal of inherited metabolic disease → ACNP
ISSN journal
01418955
Volume
20
Issue
6
Year of publication
1997
Pages
833 - 834
Database
ISI
SICI code
0141-8955(1997)20:6<833:TLEOAC>2.0.ZU;2-L