Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease (Q24679112)
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Current Data About Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease
(P31) (Q13442814)

(Q2782326)

(P50) (Q53426763)
(P1932) C Toomes
(P1545) 8

(Q82048083)
(P1545) 2
(P1932) J E Craig

(P304) e47

(P407) (Q1860)

(P433) 8

(P478) 39

(P577) +2002-08-00T00:00:00Z

(P921) (Q852654)

(Q3629049)
(P887)

(P1433) (Q14640281)

(P1476) "Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease" (language: en)

(P2093) N J Marchbank
(P1545) 1

J P Leek
(P1545) 3

M Toohey
(P1545) 4

A J Churchill
(P1545) 5

A F Markham
(P1545) 6

D A Mackey
(P1545) 7

C F Inglehearn
(P1545) 9

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External Links
(P356) 10.1136/JMG.39.8.E47
(P698) 12161614
(P932) 1735190
(P3181) 4256940
(P5875) 277497280