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Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome
by
Igelman, Austin D
,
Ku, Cristy
,
da Palma, Mariana Matioli
,
Georgiou, Michalis
,
Schiff, Elena R
,
Lam, Byron L
,
Sankila, Eeva-Marja
,
Ahn, Jeeyun
,
Pyers, Lindsey
,
Vincent, Ajoy
,
Ferraz Sallum, Juliana Maria
,
Zein, Wadih M
,
Oh, Jin Kyun
,
Maldonado, Ramiro S
,
Ryu, Joseph
,
Tsang, Stephen H
,
Gorin, Michael B
,
Webster, Andrew R
,
Michaelides, Michel
,
Yang, Paul
,
Pennesi, Mark E
Published in
Ophthalmic genetics
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Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome
by
Igelman, Austin D.
,
Ku, Cristy
,
da Palma, Mariana Matioli
,
Georgiou, Michalis
,
Schiff, Elena R.
,
Lam, Byron L.
,
Sankila, Eeva-Marja
,
Ahn, Jeeyun
,
Pyers, Lindsey
,
Vincent, Ajoy
,
Ferraz Sallum, Juliana Maria
,
Zein, Wadih M.
,
Oh, Jin Kyun
,
Maldonado, Ramiro S.
,
Ryu, Joseph
,
Tsang, Stephen H.
,
Gorin, Michael B.
,
Webster, Andrew R.
,
Michaelides, Michel
,
Yang, Paul
,
Pennesi, Mark E.
Published in
Ophthalmic Genetics
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Ophthalmic Genetics
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Subjects
Abhd12
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Arsg
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Atypical Usher Syndrome
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Cep250
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Cep78
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Adolescent
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Arylsulfatases - Genetics
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Autoantigens - Genetics
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Cell Cycle Proteins - Genetics
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Codon, Nonsense - Genetics
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Cone-Rod Dystrophies - Diagnosis
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Cone-Rod Dystrophies - Genetics
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Female
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Genetic Testing
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Genetics & Heredity
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Hearing Loss, Sensorineural - Diagnosis
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Hearing Loss, Sensorineural - Genetics
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Taylor And Francis:jisc Collections:taylor And Francis Read And Publish Agreement 2024-2025:Medical Collection (Reading List)
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