Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease [2]

K. Barada; G. Nemer; I. I. Elhajj; J. Touma; N. Cortas; R. M. Boustany; Julnar Usta

doi:10.1111/j.1399-0004.2007.00853.x

Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease [2]

K. Barada
, G. Nemer
, I. I. Elhajj
, J. Touma
, N. Cortas
, R. M. Boustany
, Julnar Usta^*

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

11 Citations (Scopus)

Original language	English
Pages (from-to)	264-267
Number of pages	4
Journal	Clinical Genetics
Volume	72
Issue number	3
DOIs	https://doi.org/10.1111/j.1399-0004.2007.00853.x
Publication status	Published - Sept 2007
Externally published	Yes

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10.1111/j.1399-0004.2007.00853.x

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@article{eb28963832be4808a7441f8ebf260c4e,

title = "Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease [2]",

author = "K. Barada and G. Nemer and Elhajj, \{I. I.\} and J. Touma and N. Cortas and Boustany, \{R. M.\} and Julnar Usta",

year = "2007",

month = sep,

doi = "10.1111/j.1399-0004.2007.00853.x",

language = "English",

volume = "72",

pages = "264--267",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "3",

}

TY - JOUR

T1 - Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease [2]

AU - Barada, K.

AU - Nemer, G.

AU - Elhajj, I. I.

AU - Touma, J.

AU - Cortas, N.

AU - Boustany, R. M.

AU - Usta, Julnar

PY - 2007/9

Y1 - 2007/9

UR - https://www.scopus.com/pages/publications/34548138877

U2 - 10.1111/j.1399-0004.2007.00853.x

DO - 10.1111/j.1399-0004.2007.00853.x

M3 - Letter

C2 - 17718866

AN - SCOPUS:34548138877

SN - 0009-9163

VL - 72

SP - 264

EP - 267

JO - Clinical Genetics

JF - Clinical Genetics

IS - 3

ER -

Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease [2]

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