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Search Results - O'Regan, Jeremiah P.
Search Results - O'Regan, Jeremiah P.
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
by
Rosen, Daniel R.
,
Siddique, Teepu
,
Patterson, David
,
Figlewicz, Denise A.
,
Sapp, Peter
,
Hentati, Afif
,
Donaldson, Deirdre
,
Goto, Jun
,
O'Regan, Jeremiah P.
,
Deng, Han-Xiang
,
Rahmani, Zohra
,
Krizus, Aldis
,
McKenna-Yasek, Diane
,
Cayabyab, Annarueber
,
Gaston, Sandra M.
,
Berger, Ralph
,
Tanzi, Rudolph E.
,
Halperin, John J.
,
Herzfeldt, Brian
,
Van den Bergh, Raymond
,
Hung, Wu-Yen
,
Bird, Thomas
,
Deng, Gang
,
Mulder, Donald W.
,
Smyth, Celestine
,
Laing, Nigel G.
,
Soriano, Edwin
,
Pericak–Vance, Margaret A.
,
Haines, Jonathan
,
Rouleau, Guy A.
,
Gusella, James S.
,
Horvitz, H. Robert
,
Brown, Robert H.
Published in
Nature (London)
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Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis
by
Esteban, Jesus
,
Rosen, Daniel R.
,
Bowling, Allen C.
,
Sapp, Peter
,
McKenna-Yasek, D.
,
O'Regan, Jeremiah P.
,
Beal, M.Flint
,
Horvitz, H.Robert
,
Brown, Robert H.
Published in
Human molecular genetics
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Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosis
by
Sapp, P C
,
Rosen, D R
,
Hosler, B A
,
Esteban, J
,
McKenna-Yasek, D
,
O'Regan, J P
,
Horvitz, H R
,
Brown, Jr, R H
Published in
Neuromuscular disorders : NMD
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Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21
by
Gregor, P
,
Gaston, S M
,
Yang, X
,
O'Regan, J P
,
Rosen, D R
,
Tanzi, R E
,
Patterson, D
,
Haines, J L
,
Horvitz, H R
,
Uhl, G R
Published in
Human genetics
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Identification of three novel mutations in the gene for CuZn superoxide dismutase in patients with familial amyotrophic lateral sclerosis
by
Sapp, Peter C
,
Rosen, Daniel R
,
Hosler, Betsy A
,
Esteban, Jesus
,
McKenna-Yasek, Diane
,
O'regan, Jeremiah P
,
Horvitz, H.Robert
,
Brown, Robert H
Published in
Neuromuscular disorders : NMD
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Identification of three novel mutations in the gene for [formula omitted] superoxide dismutase in patients with familial amyotrophic lateral sclerosis
by
Sapp, Peter C
,
Rosen, Daniel R
,
Hosler, Betsy A
,
Esteban, Jesus
,
McKenna-Yasek, Diane
,
O'regan, Jeremiah P
,
Horvitz, H.Robert
,
Brown, Robert H
Published in
Neuromuscular disorders : NMD
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Neuromuscular Disorders : Nmd
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Superoxide Dismutase - Genetics
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