Wikidata

(Q43196100)

English

MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion.

scientific article published on 31 December 2009

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Statements

title
MTHFR C677T homozygous mutation in a patient with pigmentary glaucoma and central retinal vein occlusion (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
20068371
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068371%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020

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