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Connection

Edwardo Ramos to Mutation

This is a "connection" page, showing publications Edwardo Ramos has written about Mutation.
Connection Strength

1.079
  1. Ramos E, Pardo S, Mas Rodr?guez MF, V?lez J. Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene. J Clin Neuromuscul Dis. 2015 Dec; 17(2):59-62.
    View in: PubMed
    Score: 0.378
  2. Noriega E, Ramos E. New mutation in periaxin gene causing Charcot Marie Tooth disease in a Puerto Rican young male. J Clin Neuromuscul Dis. 2013 Dec; 15(2):63-8.
    View in: PubMed
    Score: 0.329
  3. Otero-Loperena E, Ortiz-Santiago A, Ramos E. Familial Hyperckemia and Calf Hypertrophy Secondary to a Caveolin-3 Mutation. Am J Phys Med Rehabil. 2021 07 01; 100(7):e101-e103.
    View in: PubMed
    Score: 0.139
  4. Ortiz-Santiago A, Ramos E. Childhood onset homozygous recessive GDAP1 (p.Pro231Leu) mutation in a 9-year-old puerto rican pediatric female with axonal Charcot-Marie-Tooth disease: A case report. J Pediatr Rehabil Med. 2021; 14(3):533-537.
    View in: PubMed
    Score: 0.135
  5. Ramos E, Conde JG, Berrios RA, Pardo S, G?mez O, Mas Rodr?guez MF. Prevalence and Genetic Profile of Duchene and Becker Muscular Dystrophy in Puerto Rico. J Neuromuscul Dis. 2016 05 27; 3(2):261-266.
    View in: PubMed
    Score: 0.098
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.
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