Mizuo-Nakamura phenomenon in cone-rod dystrophy

被引：2

作者：

Kumar, Vinod ^{[1
]}

Goel, Neha ^{[2
]}

Bhaskaran, Ullattil K. ^{[1
]}

Garg, Itika ^{[1
]}

机构：

[1] All India Inst Med Sci, Dr Rajendra Prasad Ctr Ophthalm Sci, New Delhi, India

[2] ICARE Eye Hosp & Postgrad Inst, Noida, Uttar Pradesh, India

来源：

关键词：

colour vision; cone-rod dystrophy; Mizuo-Nakamura phenomenon; retina; GENE;

D O I：

10.1111/cxo.12491

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

[No abstract available]

引用

页码：388 / 391

页数：4

共 11 条

[1] MIZUO PHENOMENON IN X-LINKED RETINOSCHISIS - PATHOGENESIS OF THE MIZUO PHENOMENON
DEJONG, PTVM
ZRENNER, E
VANMEEL, GJ
KEUNEN, JEE
VANNORREN, D
[J]. ARCHIVES OF OPHTHALMOLOGY, 1991, 109 (08) : 1104 - 1108
[2] A HOMOZYGOUS 1-BASE PAIR DELETION IN THE ARRESTIN GENE IS A FREQUENT CAUSE OF OGUCHI DISEASE IN JAPANESE
FUCHS, S
NAKAZAWA, M
MAW, M
TAMAI, M
OGUCHI, Y
GAL, A
[J]. NATURE GENETICS, 1995, 10 (03) : 360 - 362
[3] Cone rod dystrophies
Hamel, Christian P.
[J]. ORPHANET JOURNAL OF RARE DISEASES, 2007, 2 (1)
[4] X-LINKED RECESSIVE CONE DYSTROPHY WITH TAPETAL-LIKE SHEEN - A NEWLY RECOGNIZED ENTITY WITH MIZUO-NAKAMURA PHENOMENON
HECKENLIVELY, JR
WELEBER, RG
[J]. ARCHIVES OF OPHTHALMOLOGY, 1986, 104 (09) : 1322 - 1328
[5] KRILL AE, 1973, DOC OPHTHALMOL, V35, P1
[6] ISCEV Standard for full-field clinical electroretinography (2015 update)
McCulloch, Daphne L.
Marmor, Michael F.
Brigell, Mitchell G.
Hamilton, Ruth
Holder, Graham E.
Tzekov, Radouil
Bach, Michael
[J]. DOCUMENTA OPHTHALMOLOGICA, 2015, 130 (01) : 1 - 12
[7] Mizuo G, 1913, ACTA SOC OPHTHALMOL, V17, P1148
[8] NAKAMURA B, 1920, KLIN MONATSBL AUGENH, V65, P83
[9] Oguchi C., 1907, NIPPON GANKAKAI ZASS, V11, P123
[10] Salcedo-Villanueva Guillermo, 2013, Retin Cases Brief Rep, V7, P259, DOI 10.1097/ICB.0b013e31828eef5d