Literature DB >> 1822810

Clinical and genetic heterogeneity in spinal muscular atrophy--the multiple allele model.

A E Emery.   

Abstract

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Year:  1991        PMID： 1822810     DOI： 10.1016/0960-8966(91)90106-3

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN： 0960-8966            Impact factor:   4.296


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  5 in total

Review 1.  Molecular genetics of autosomal recessive spinal muscular atrophy.

Authors:  N R Rodrigues; K Talbot; K E Davies
Journal:  Mol Med       Date:  1996-07       Impact factor: 6.354

2.  Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype.

Authors:  L Campbell; A Potter; J Ignatius; V Dubowitz; K Davies
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

3.  Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy.

Authors:  K Talbot; N Rodrigues; G Bernert; R Bittner; K Davies
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

4.  The neuronal apoptosis inhibitory protein is a direct inhibitor of caspases 3 and 7.

Authors:  Johannes K X Maier; Zahia Lahoua; Nathalie H Gendron; Raouf Fetni; Anne Johnston; Jamshid Davoodi; Dita Rasper; Sophie Roy; Ruth S Slack; Donald W Nicholson; Alex E MacKenzie
Journal:  J Neurosci       Date:  2002-03-15       Impact factor: 6.167

5.  Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Authors:  A M Theodosiou; K E Morrison; A M Nesbit; R J Daniels; L Campbell; M J Francis; Z Christodoulou; K E Davies
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025
  5 in total

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