Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

[1]  M. Pericak-Vance,et al.  Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. , 1993, Science.

[2]  J. Haines,et al.  Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis , 1993, Nature.

[3]  M C Speer,et al.  A microsatellite genetic linkage map of human chromosome 18. , 1993, Genomics.

[4]  M. Pericak-Vance,et al.  Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q , 1992, Nature Genetics.

[5]  G. Gyapay,et al.  A second-generation linkage map of the human genome , 1992, Nature.

[6]  H. Sies.  Oxidative stress: from basic research to clinical application. , 1991, The American journal of medicine.

[7]  J. Haines,et al.  Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. , 1991, The New England journal of medicine.

[8]  J. Weber,et al.  Dinucleotide repeat polymorphism at the PENK locus. , 1990, Nucleic acids research.

[9]  J. Weber,et al.  Dinucleotide repeat polymorphism at the D2S72 locus. , 1990, Nucleic acids research.

[10]  M. Lathrop,et al.  Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q , 1990, Nature.

[11]  M. Hamida,et al.  Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy. , 1990, Brain : a journal of neurology.

[12]  M. Pericak-Vance,et al.  Linkage analysis in familial amyotrophic lateral sclerosis , 1989, Neurology.

[13]  J. Weber,et al.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.

[14]  R. Malina,et al.  Genetic drift and natural selection in an isolated Zapotec-speaking community in the Valley of Oaxaca, southern Mexico. , 1989, Human heredity.

[15]  M. Lefranc,et al.  Human Ig superfamily CTLA‐4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA‐4 cytoplasmic domains , 1988, European journal of immunology.

[16]  M. Hamida,et al.  Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis , 1987, Journal of the Neurological Sciences.

[17]  E. Lander,et al.  Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[18]  M. Ben Hamida,et al.  [Charcot's disease and juvenile amyotrophic lateral sclerosis]. , 1984, Revue neurologique.