Connection

TETSUO ASHIZAWA to Myotonia Congenita

This is a "connection" page, showing publications TETSUO ASHIZAWA has written about Myotonia Congenita.
Connection Strength

0.406
  1. A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene. Neurology. 2000 Dec 12; 55(11):1697-703.
    View in: PubMed
    Score: 0.182
  2. Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene. Rev Biol Trop. 2008 Mar; 56(1):1-11.
    View in: PubMed
    Score: 0.075
  3. Gene symbol: CLCN1. Disease: Myotonia congenita. Hum Genet. 2008 Feb; 123(1):104-5.
    View in: PubMed
    Score: 0.075
  4. Novel human pathological mutations. Gene symbol: CLCN1. Disease: myotonia congenita, autosomal recessive. Hum Genet. 2007 Nov; 122(3-4):413.
    View in: PubMed
    Score: 0.073
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.