The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences-Reference-Cited by-同舟云学术

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The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

Published:1996-12-01 Issue:12 Volume:5 Page:1915-1920
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Ma L

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/12/1915/1860521/5-12-1915.pdf

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