Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease

AJ Churchill, NJ Marchbank, J Craig, J Leek, M Toohey, AJ Markham, D Mackey, C Toomes, CF Inglehearn

Research output: Contribution to journal › Article (Academic Journal) › peer-review

Translated title of the contribution	Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease
Original language	English
Pages (from-to)	47 - 48
Journal	Journal of Medical Genetics
Volume	39
Publication status	Published - 2002

Handle.net

@article{55a5fa3bd1a24b2ca2816c92af95019f,

title = "Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease",

author = "AJ Churchill and NJ Marchbank and J Craig and J Leek and M Toohey and AJ Markham and D Mackey and C Toomes and CF Inglehearn",

year = "2002",

language = "English",

volume = "39",

pages = "47 -- 48",

journal = "Journal of Medical Genetics",

issn = "1468-6244",

publisher = "BMJ Publishing Group",

}

TY - JOUR

T1 - Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease

AU - Churchill, AJ

AU - Marchbank, NJ

AU - Craig, J

AU - Leek, J

AU - Toohey, M

AU - Markham, AJ

AU - Mackey, D

AU - Toomes, C

AU - Inglehearn, CF

PY - 2002

Y1 - 2002

M3 - Article (Academic Journal)

SN - 1468-6244

VL - 39

SP - 47

EP - 48

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

ER -