Robert Wollmann to Base Sequence
This is a "connection" page, showing publications Robert Wollmann has written about Base Sequence.
Connection Strength
0.117
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Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia. Clin Genet. 2014 Feb; 85(2):166-71.
Score: 0.085
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LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. Hum Genet. 2012 Jul; 131(7):1123-35.
Score: 0.019
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Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions. Am J Hum Genet. 1996 Aug; 59(2):400-6.
Score: 0.007
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CNS gene delivery by retrograde transport of recombinant replication-defective adenoviruses. Gene Ther. 1995 Mar; 2(2):132-7.
Score: 0.006