Mutation in the pleckstrin homology domain of the human phospholipase C-δ1 gene is associated with loss of function

Biochemical and Biophysical Research Communications

Volumn 245, Issue 3, 1998, Pages 722-728

  Shimohama, Shun ^a   Kamiya, Shinji ^b   Fujii, Makoto ^c   Ogawa, Tetsuo ^c   Kanamori, Mutsumi ^c   Kawamata, Jun ^a   Imura, Tetsuya ^a   Taniguchi, Takashi ^b   Yagisawa, Hitoshi ^c  

^a KYOTO UNIVERSITY   (Japan)

^b KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

^c UNIVERSITY OF HYOGO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTATHIONE TRANSFERASE; HYBRID PROTEIN; INOSITOL 1,4,5 TRISPHOSPHATE; PHOSPHOLIPASE C; PLECKSTRIN;

AMINO ACID SUBSTITUTION; ARTICLE; BINDING AFFINITY; CONFORMATIONAL TRANSITION; ENZYME INHIBITION; GENE MUTATION; MISSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS;

MAMMALIA;

EID: 0032576970     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1998.8307     Document Type: Article

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