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Autor:
M. Ashwin Reddy, Shomi S. Bhattacharya, Eranga N. Vithana, Vanita Berry, Roy A. Quinlan, Peter J. Francis, Gary Dawson, Ian Mackay, Alisoun H. Carey, Dean Collyer, Anthony T. Moore
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
American journal of human genetics, 2001, Vol.69(5), pp.1141-1145 [Peer Reviewed Journal]
instname
American journal of human genetics, 2001, Vol.69(5), pp.1141-1145 [Peer Reviewed Journal]
5 páginas, 4 figuras.-- et al.
Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to chromosome 11q22-q22
Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to chromosome 11q22-q22
Autor:
Ian Mackay, Eranga N. Vithana, Vanita Berry, Anthony T. Moore, Roy A. Quinlan, Dean Collyer, Alisoun H. Carey, M. Ashwin Reddy, Shomi S. Bhattacharya, Peter J. Francis, Gary Dawson
To the Editor:We thank Dr. Siiri Veromann (Veromann 2002xTheoretical considerations regarding the study “Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans.”. Veromann, S. Am J Hum Genet. 2002;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be5048237cb61ef4ffea245d701e04a
https://europepmc.org/articles/PMC379207/
https://europepmc.org/articles/PMC379207/