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3 results for author:"Gill S.P." in Literature citations

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Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia.

Cuajungco M.P., Leyne M., Mull J., Gill S.P., Lu W., Zagzag D., Axelrod F.B., Maayan C., Gusella J.F., Slaugenhaupt S.A.

Am. J. Hum. Genet. 72:749-758(2003) · Mapped (9)

Cloning, characterization, and genomic structure of the mouse Ikbkap gene.

Cuajungco M.P., Leyne M., Mull J., Gill S.P., Gusella J.F., Slaugenhaupt S.A.

DNA Cell Biol. 20:579-586(2001) · UniProtKB (1) · Mapped (24)

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia.

Slaugenhaupt S.A., Blumenfeld A., Gill S.P., Leyne M., Mull J., Cuajungco M.P., Liebert C.B., Chadwick B.P., Idelson M., Reznik L. et al.

Am. J. Hum. Genet. 68:598-605(2001) · UniProtKB (1) · Mapped (3)

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