G. Hobson
发表
J. Lupski,
Jennifer A. Lee,
J. Garbern,
2006,
Annals of neurology.
Vladimir G. Gainullin,
E. Bertini,
A. Vanderver,
2020,
Annals of clinical and translational neurology.
J. Garbern,
Grace M Hobson,
James Y Garbern,
2012,
Seminars in Neurology.
N. Carter,
H. Heng,
M. Ross,
2005,
American journal of human genetics.
S. Naidu,
P. Rogan,
E. Sistermans,
2006,
Human mutation.
A. Fattal-Valevski,
F. Hisama,
J. Garbern,
2009,
Journal of child neurology.
R. Horlick,
G. Hobson,
P. Benfield,
1990,
Molecular and cellular biology.
J. Lupski,
S. Cheung,
F. Zhang,
2020,
Human mutation.
E. Bertini,
M. Tarnopolsky,
C. Catsman-Berrevoets,
2015,
Annals of clinical and translational neurology.
K.,
Stevens,
A. Vanderver,
2020,
The Journal of clinical endocrinology and metabolism.
R. Tuan,
V. Funanage,
I. Shapiro,
1999,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
Joshua L. Deignan,
Lora J. H. Bean,
J. Rosenfeld,
2020,
American journal of medical genetics. Part A.
G. Molloy,
G. Hobson,
P. Benfield,
1990,
Molecular and cellular biology.
M. Pearson,
G. Hobson,
P. Benfield,
1988,
Gene.
G. Hobson,
P. Benfield,
P. Harlow,
1996,
Methods in molecular biology.
M. Shy,
J. Kamholz,
J. Garbern,
2001,
Neurology.
V. Funanage,
R. Stanton,
P. A. Moses,
1999,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
R. Skoff,
C. Landel,
K. Sperle,
2013,
The Journal of Neuroscience.
J. Rosenfeld,
J. Lupski,
R. Gibbs,
2022,
American journal of human genetics.
G. Molloy,
G. Hobson,
P. Benfield,
1990
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A. Vanderver,
J. Soul,
K. Maski,
2014,
Molecular genetics and metabolism.
E. Hoffman,
C. Angelini,
M. Cadaldini,
1996,
Neurology.
J. Lupski,
K. Woodward,
Vahid Bahrambeigi,
2019,
Genome Medicine.
Suzanne M. McCahan,
J. Lupski,
C. Carvalho,
2015,
PLoS genetics.
A. Vanderver,
J. Bouchard,
C. Toro,
2013,
Human mutation.
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease.
K. Woodward,
R. Surtees,
M. Endzinienė,
2005,
Brain : a journal of neurology.
M. Zatz,
F. Cambi,
G. Hobson,
2002,
American journal of medical genetics.
J. Golden,
T. Bird,
R. Woltjer,
2009,
Acta Neuropathologica.
S. Waldman,
T. Shaffer,
Yan Zhu,
2015,
Pulmonary pharmacology & therapeutics.
E. Wang,
F. Cambi,
N. Dimova,
2006,
Journal of cellular biochemistry.
P. Seeman,
J. Garbern,
K. Sperle,
2014,
Human molecular genetics.
Neil A. Miller,
S. Kingsmore,
E. Farrow,
2012
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Jennifer Kirkham,
Alan H Brook,
J. Kirkham,
2009,
American journal of medical genetics. Part A.
J. Kamholz,
G. Hobson,
2013
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G. Hobson,
E. Selva,
Kristi Clark,
2011
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S. Hopkins,
T. Morlet,
K. Nagao,
2018,
Journal of Neurology.
G. Molloy,
M. Pearson,
G. Hobson,
1988,
Nucleic acids research.
H. Marks,
F. Cambi,
D. Stabley,
2002,
Annals of neurology.
R. Krahe,
R. Roberts,
J. Durand,
1997,
Molecular and cellular probes.
R. Kinkel,
M. Golomb,
B. Darras,
2007,
Neurology.
G. Hobson,
P. Benfield,
P. Harlow,
1996,
Methods in molecular biology.
G. Hobson,
P. Benfield,
P. Harlow,
1994,
Methods in molecular biology.
Daniel C. Factor,
S. Goldman,
V. Fossati,
2017,
American journal of human genetics.
E. Bertini,
M. Shy,
J. Kamholz,
2003,
Annals of neurology.
I. D. de Coo,
V. Funanage,
H. Marks,
2000,
Neurology.
K. Sperle,
G. Hobson,
J. Taube,
2018,
Molecular therapy. Nucleic acids.
E. Wang,
F. Cambi,
N. Dimova,
2008,
Experimental Neurology.
A case of complicated spastic paraplegia 2 due to a point mutation in the proteolipid protein 1 gene
Eun Sil Lee,
H. Moon,
J. Garbern,
2004,
Journal of the Neurological Sciences.
M. Siciliano,
V. Funanage,
R. Krahe,
1995,
Genomics.
G. Hobson,
P. Benfield,
M. Mitchell,
1992,
The Journal of biological chemistry.
E. Wang,
F. Cambi,
N. Dimova,
2008,
Experimental Neurology.