DOI: 10.1086/302955. Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

10.1086/302955

Crossref journal-article

Elsevier BV

The American Journal of Human Genetics (78)

Bibliography

Crow, Y. J., Jackson, A. P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C. D., Hamel, B. C. J., Jayatunga, R., Karbani, G., KÃ¡lmÃ¡nchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., â¦ Woods, C. G. (2000). Aicardi-GoutiÃ¨res Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21. The American Journal of Human Genetics, 67(1), 213â221.

Authors 26

Y.J. Crow (first)
A.P. Jackson (additional)
E. Roberts (additional)
E. van Beusekom (additional)
P. Barth (additional)
P. Corry (additional)
C.D. Ferrie (additional)
B.C.J. Hamel (additional)
R. Jayatunga (additional)
G. Karbani (additional)
R. Kálmánchey (additional)
A. Kelemen (additional)
M. King (additional)
R. Kumar (additional)
J. Livingstone (additional)
R. Massey (additional)
R. McWilliam (additional)
A. Meager (additional)
C. Rittey (additional)
J.B.P. Stephenson (additional)
J.L. Tolmie (additional)
A. Verrips (additional)
T. Voit (additional)
H. van Bokhoven (additional)
H.G. Brunner (additional)
C.G. Woods (additional)

References 37 Referenced 65

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10.1097/00019605-199804000-00009 / Clin Dysmorphol / The autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcification, and CNS disease: report of another Bedouin family by al-Dabbous (1998)
10.1111/j.1365-2133.1996.tb01521.x / Br J Dermatol / Raynaud's phenomenon and digital necrosis induced by interferon-alpha by Bachmeyer (1996)
10.1136/jmg.20.3.210 / J Med Genet / Microcephaly and intracranial calcification in two brothers by Baraitser (1983)
10.1007/s004010051071 / Acta Neuropathol / Aicardi-Goutières syndrome: a genetic microangiopathy? by Barth (1999)
10.1055/s-2008-1071412 / Neuropediatrics / Magnetic resonance imaging in infantile encephalopathy with cerebral calcification and leukodystrophy by Bolthauser (1991)
10.1055/s-2008-1071333 / Neuropediatrics / Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis—another case of the Aicardi-Goutières syndrome by Bönnemann (1992)
10.1111/j.1399-0004.1986.tb00578.x / Clin Genet / A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection by Burn (1986)
10.1016/S0006-8993(99)01328-1 / Brain Res / Structural and functional neuropathology in transgenic mice with CNS expression of IFN-α by Campbell (1999)
10.1159/000017917 / Dermatology / Acrocyanosis induced by interferon α2a by Campo-Voegeli (1998)
10.1002/1529-0131(199905)42:5<1051::AID-ANR26>3.0.CO;2-Q / Arthritis Rheum / Interferon-α may exacerbate cryoglobulinemia-related ischaemic manifestations: an adverse effect potentially related to its anti-angiogenic activity by Cid (1999)
10.1177/000331979604700210 / Angiology / Severe Raynaud's syndrome associated with interferon therapy: a case history by Creutzig (1996)
10.1590/S0004-282X1986000200011 / Arq Neuropsiquiatr / Syndrome of calcifications of basal ganglia, leukodystrophy and chronic lymphomonocytic pleocytosis of the cerebrospinal fluid: report of a case by Diament (1986)
10.1034/j.1399-0004.1999.560210.x / Clin Genet / Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease? by Fauré (1999)
10.1046/j.1365-2893.1998.00103.x / J Viral Hepat / Are all type I human interferons equivalent? by Foster (1998)
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Dates

Type	When
Created	23 years, 1 month ago (July 26, 2002, 2:47 p.m.)
Deposited	2 years, 4 months ago (April 22, 2023, 7:02 p.m.)
Indexed	2 months, 2 weeks ago (June 13, 2025, 5:42 a.m.)
Issued	25 years, 1 month ago (July 1, 2000)
Published	25 years, 1 month ago (July 1, 2000)
Published Print	25 years, 1 month ago (July 1, 2000)

Funders 0

None

BibTeX

@article{Crow_2000, title={Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21}, volume={67}, ISSN={0002-9297}, url={http://dx.doi.org/10.1086/302955}, DOI={10.1086/302955}, number={1}, journal={The American Journal of Human Genetics}, publisher={Elsevier BV}, author={Crow, Y.J. and Jackson, A.P. and Roberts, E. and van Beusekom, E. and Barth, P. and Corry, P. and Ferrie, C.D. and Hamel, B.C.J. and Jayatunga, R. and Karbani, G. and Kálmánchey, R. and Kelemen, A. and King, M. and Kumar, R. and Livingstone, J. and Massey, R. and McWilliam, R. and Meager, A. and Rittey, C. and Stephenson, J.B.P. and Tolmie, J.L. and Verrips, A. and Voit, T. and van Bokhoven, H. and Brunner, H.G. and Woods, C.G.}, year={2000}, month=jul, pages={213–221} }

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