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Hufnagel, R.B
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Hufnagel, R.B
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Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease
by
Allikmets, R.
,
Brooks, B.P
,
Chen, R.
,
Fishman, G.A
,
Goetz, K.
,
Hufnagel
,
R.B
,
Lee, W.
,
Nagasaki, T.
,
Su, P.-Y
,
Tsang, S.H
,
Tumminia, S.J
,
Ullah, E.
,
Wang, J.
,
Zernant, J.
Published 2022
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Related Subjects
ABC transporter
ABCA4 protein, human
ATP-Binding Cassette Transporters
Eye Proteins
Gene Frequency
Humans
Macular Degeneration
Mutation
Pedigree
Phenotype
ROM1 protein, human
Stargardt Disease
Stargardt disease
Tetraspanins
eye protein
gene frequency
genetics
human
macular degeneration
mutation
pedigree
phenotype
tetraspanin
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