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1 .
Author reply: To PMID 24480711
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by
Stephanie, Halford
;
Gerald, Liew
;
Donna S, Mackay
;
Panagiotis I, Sergouniotis
;
Richard, Holt
, et al.
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Ophthalmology
. 122(4)
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7 .
RDH12 retinopathy: novel mutations and phenotypic description
저자
by
Donna S, Mackay
;
Arundhati, Dev Borman
;
Phillip, Moradi
;
Robert H, Henderson
;
Zheng, Li
, et al.
소스
Molecular Vision
Open Access (OpenAIRE)
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7 .
Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans
저자
by
Robert H, Henderson
;
Zheng, Li
;
Mai M, Abd El Aziz
;
Donna S, Mackay
;
Mohammad A, Eljinini
, et al.
소스
Molecular Vision
Open Access (OpenAIRE)
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7 .
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant 'nuclear punctate' cataracts linked to chromosome 13q
저자
by
Thomas M, Bennett
;
Donna S, Mackay
;
Harry L S, Knopf
;
Alan, Shiels
.
소스
Molecular vision
. 10
Open Access (OpenAIRE)
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6 .
A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant 'coral-like' cataract linked to chromosome 2q
저자
by
Donna S, Mackay
;
Usha P, Andley
;
Alan, Shiels
.
소스
Molecular vision
. 10
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5 .
Galactokinase gene mutations and age-related cataract. Lack of association in an Italian population
저자
by
Giovanni, Maraini
;
J Fielding, Hejtmancik
;
Alan, Shiels
;
Donna S, Mackay
;
Raffaella, Aldigeri
, et al.
소스
Molecular vision
. 9
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