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Connection

Frida Kleiman to Hexosaminidase B

This is a "connection" page, showing publications Frida Kleiman has written about Hexosaminidase B.
Connection Strength

0.073
  1. Kleiman FE, Ram?rez AO, Dodelson de Kremer R, Gravel RA, Argara?a CE. A frequent TG deletion near the polyadenylation signal of the human HEXB gene: occurrence of an irregular DNA structure and conserved nucleotide sequence motif in the 3' untranslated region. Hum Mutat. 1998; 12(5):320-9.
    View in: PubMed
    Score: 0.041
  2. Kleiman FE, de Kremer RD, de Ramirez AO, Gravel RA, Argara?a CE. Sandhoff disease in Argentina: high frequency of a splice site mutation in the HEXB gene and correlation between enzyme and DNA-based tests for heterozygote detection. Hum Genet. 1994 Sep; 94(3):279-82.
    View in: PubMed
    Score: 0.032
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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