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1 .
Absence of previously reported variants in theSCNA (G88C and G209A),NR4A2 (T291D and T245G) and theDJ-1 (T497C) genes in familial Parkinson's disease from theGenePD study
저자
by
Christine Klein
;
Margery H. Mark
;
Robert G. Feldman
;
Mark F. Lew
;
Marie Saint-Hilaire
, et al.
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Movement Disorders
. 20:1188-1191
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7 .
Clinical genetic analysis of Parkinson's disease in the contursi kindred
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by
G. Sanges
;
Lawrence I. Golbe
;
Salvatore la Sala
;
Roger C. Duvoisin
;
Vincenzo Bonavita
, et al.
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Annals of Neurology
. 40:767-775
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7 .
Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23
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by
G. Sanges
;
Roger C. Duvoisin
;
Lana T. Pho
;
Alejandro A. Schäffer
;
Giuseppe Di Iorio
, et al.
소스
Science
. 274:1197-1199
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7 .
Segregation analysis of Parkinson disease revealing evidence for a major causative gene
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by
G. F. Wooten
;
Lawrence I. Golbe
;
Lillian J. Currie
;
Robert G. Feldman
;
Alice M. Lazzarini
, et al.
소스
American journal of medical genetics
. 109(3)
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7 .
Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis
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by
N. Zhong
;
Edward S. Stenroos
;
Thomas Wisniewski
;
Wojciech Kaczmarski
;
Alice M. Lazzarini
, et al.
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Annals of neurology
. 43(1)
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7 .
Attitudes regarding utilization of artificial insemination by donor in Huntington disease
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by
Alice M. Lazzarini
;
Laurence E. Karp
;
Sandra R. Leiblum
;
John Optiz
;
Michael K. McCormack
.
소스
American journal of medical genetics
. 14(1)
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