A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)-Reference-Cited by-同舟云学术

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A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)

Published:2004-03-03 Issue:9 Volume:13 Page:975-981
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Fossdal R.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/13/9/975/1612825/ddh106.pdf

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