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Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson’s disease
Author(s) -
Barada K,
Nemer G,
ElHajj II,
Touma J,
Cortas N,
Boustany RM,
Usta J
Publication year - 2007
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2007.00853.x
Subject(s) - medicine , pediatric gastroenterology , family medicine , disease