Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2) | British Journal of Ophthalmology

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This article has a correction. Please see:

CORRECTIONS - February 01, 2004

Clinical science

Scientific reports

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2)

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Cite this article as:: Michaelides M, Aligianis IA, Holder GE, et al

Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2)

British Journal of Ophthalmology 2003;87:1317-1320.