Clinical spectrum of vitreoretinal lymphoma and its association with MyD88 L265P mutation

Ester Carreno; Tim Clench; Laura R Steeples; Serena Salvatore; Richard W J Lee; Andrew D Dick; Joya Pawade

doi:10.1111/aos.13808

Clinical spectrum of vitreoretinal lymphoma and its association with MyD88 L265P mutation

Ester Carreno^*
, Tim Clench
, Laura R Steeples
, Serena Salvatore
, Richard W J Lee
, Andrew D Dick
, Joya Pawade

^*Corresponding author for this work

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

14 Citations (Scopus)

Abstract

[No abstract]

Original language	English
Pages (from-to)	e138-e139
Journal	Acta Ophthalmologica
Volume	97
Issue number	1
Early online date	16 Aug 2018
DOIs	https://doi.org/10.1111/aos.13808
Publication status	Published - 1 Feb 2019

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@article{79cd760cdbaf4423a9848d696fde5df5,

title = "Clinical spectrum of vitreoretinal lymphoma and its association with MyD88 L265P mutation",

abstract = "[No abstract]",

author = "Ester Carreno and Tim Clench and Steeples, \{Laura R\} and Serena Salvatore and Lee, \{Richard W J\} and Dick, \{Andrew D\} and Joya Pawade",

year = "2019",

month = feb,

day = "1",

doi = "10.1111/aos.13808",

language = "English",

volume = "97",

pages = "e138--e139",

journal = "Acta Ophthalmologica",

issn = "1755-375X",

publisher = "John Wiley and Sons Inc",

number = "1",

}

TY - JOUR

T1 - Clinical spectrum of vitreoretinal lymphoma and its association with MyD88 L265P mutation

AU - Carreno, Ester

AU - Clench, Tim

AU - Steeples, Laura R

AU - Salvatore, Serena

AU - Lee, Richard W J

AU - Dick, Andrew D

AU - Pawade, Joya

PY - 2019/2/1

Y1 - 2019/2/1

N2 - [No abstract]

AB - [No abstract]

UR - https://www.scopus.com/pages/publications/85052796966

U2 - 10.1111/aos.13808

DO - 10.1111/aos.13808

M3 - Letter (Academic Journal)

C2 - 30113125

SN - 1755-375X

VL - 97

SP - e138-e139

JO - Acta Ophthalmologica

JF - Acta Ophthalmologica

IS - 1

ER -

Clinical spectrum of vitreoretinal lymphoma and its association with MyD88 L265P mutation

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