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Author
Tsang SH
Tsang SH
References (2)
1. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome - Igelman_2021_Ophthalmic.Genet_42_664
Title :
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome -
Igelman_2021_Ophthalmic.Genet_42_664
Author(s) :
Igelman AD
,
Ku C
,
da Palma MM
,
Georgiou M
,
Schiff ER
,
Lam BL
,
Sankila EM
,
Ahn J
,
Pyers L
,
Vincent A
,
Ferraz Sallum JM
,
Zein WM
,
Oh JK
,
Maldonado RS
,
Ryu J
,
Tsang SH
,
Gorin MB
,
Webster AR
,
Michaelides M
,
Yang P
,
Pennesi ME
Ref :
Ophthalmic Genet ,
42
:664 , 2021
Abstract :
View Abstract
PubMedSearch :
Igelman_2021_Ophthalmic.Genet_42_664
PubMedID
:
34223797
Gene_locus related to this paper:
human-ABHD12
2. Impaired cholesterol efflux in retinal pigment epithelium of individuals with juvenile macular degeneration - Tsai_2021_Am.J.Hum.Genet__
Title :
Impaired cholesterol efflux in retinal pigment epithelium of individuals with juvenile macular degeneration -
Tsai_2021_Am.J.Hum.Genet__
Author(s) :
Tsai YT
,
Li Y
,
Ryu J
,
Su PY
,
Cheng CH
,
Wu WH
,
Li YS
,
Quinn PMJ
,
Leong KW
,
Tsang SH
Ref :
American Journal of Human Genetics ,
: , 2021
Abstract :
View Abstract
PubMedSearch :
Tsai_2021_Am.J.Hum.Genet__
PubMedID
:
33909993