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Editorial

. 2008 Mar;145(3):391-3.

doi: 10.1016/j.ajo.2007.12.002.

The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation syndrome

Elias I Traboulsi, Mansoor Sarfarazi

PMID: 18282488
DOI: 10.1016/j.ajo.2007.12.002

Editorial

The use of microarray technology in deciphering the cause of genetic eye diseases: LOXL1 and exfoliation syndrome

Elias I Traboulsi et al. Am J Ophthalmol. 2008 Mar.

. 2008 Mar;145(3):391-3.

doi: 10.1016/j.ajo.2007.12.002.

Authors

Elias I Traboulsi, Mansoor Sarfarazi

PMID: 18282488
DOI: 10.1016/j.ajo.2007.12.002

No abstract available

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Comment on

LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.
Fingert JH, Alward WL, Kwon YH, Wang K, Streb LM, Sheffield VC, Stone EM. Fingert JH, et al. Am J Ophthalmol. 2007 Dec;144(6):974-975. doi: 10.1016/j.ajo.2007.09.034. Am J Ophthalmol. 2007. PMID: 18036875 No abstract available.
Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population.
Hayashi H, Gotoh N, Ueda Y, Nakanishi H, Yoshimura N. Hayashi H, et al. Am J Ophthalmol. 2008 Mar;145(3):582-585. doi: 10.1016/j.ajo.2007.10.023. Epub 2008 Jan 16. Am J Ophthalmol. 2008. PMID: 18201684

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