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Connection

Afif Hentati to Base Sequence

This is a "connection" page, showing publications Afif Hentati has written about Base Sequence.
Connection Strength

0.111
  1. Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency. Ann Neurol. 1996 Mar; 39(3):295-300.
    View in: PubMed
    Score: 0.026
  2. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Hum Mol Genet. 1994 Aug; 3(8):1263-7.
    View in: PubMed
    Score: 0.023
  3. Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus. Hum Mol Genet. 1992 Jun; 1(3):218.
    View in: PubMed
    Score: 0.020
  4. Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. Am J Hum Genet. 2008 Feb; 82(2):510-5.
    View in: PubMed
    Score: 0.015
  5. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet. 2001 Oct; 29(2):160-5.
    View in: PubMed
    Score: 0.010
  6. Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis. Hum Mol Genet. 1995 Jun; 4(6):1113-6.
    View in: PubMed
    Score: 0.006
  7. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. Science. 1993 Aug 20; 261(5124):1047-51.
    View in: PubMed
    Score: 0.005
  8. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993 Mar 04; 362(6415):59-62.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.