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Search Results - Västinsalo, Hanna
Search Results - Västinsalo, Hanna
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CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development
by
Geller, Scott F
,
Guerin, Karen I
,
Visel, Meike
,
Pham, Aaron
,
Lee, Edwin S
,
Dror, Amiel A
,
Avraham, Karen B
,
Hayashi, Toshinori
,
Ray, Catherine A
,
Reh, Thomas A
,
Bermingham-McDonogh, Olivia
,
Triffo, William J
,
Bao, Shaowen
,
Isosomppi, Juha
,
Västinsalo, Hanna
,
Sankila, Eeva-Marja
,
Flannery, John G
Published in
PLoS genetics
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Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)
by
VÄSTINSALO, Hanna
,
JALKANEN, Reetta
,
DINCULESCU, Astra
,
ISOSOMPPI, Juha
,
GELLER, Scott
,
FLANNERY, John G
,
HAUSWIRTH, William W
,
SANKILA, Eeva-Marja
Published in
European journal of human genetics : EJHG
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Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane
by
Isosomppi, Juha
,
Västinsalo, Hanna
,
Geller, Scott F
,
Heon, Elise
,
Flannery, John G
,
Sankila, Eeva-Marja
Published in
Molecular vision
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Extended mutation spectrum of Usher syndrome in Finland
by
Västinsalo, Hanna
,
Jalkanen, Reetta
,
Bergmann, Carsten
,
Neuhaus, Christine
,
Kleemola, Leenamaija
,
Jauhola, Liisa
,
Bolz, Hanno Jörn
,
Sankila, Eeva‐Marja
Published in
Acta ophthalmologica (Oxford, England)
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The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A
by
Phillips, Jennifer B.
,
Västinsalo, Hanna
,
Wegner, Jeremy
,
Clément, Aurélie
,
Sankila, Eeva-Marja
,
Westerfield, Monte
Published in
Gene Expression Patterns
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Prevalence of RPGR-Mediated Retinal Dystrophy in an Unselected Cohort of Over 5000 Patients
by
Tuupanen, Sari
,
Gall, Kimberly
,
Sistonen, Johanna
,
Saarinen, Inka
,
Kämpjärvi, Kati
,
Wells, Kirsty
,
Merkkiniemi, Katja
,
von Nandelstadh, Pernilla
,
Sarantaus, Laura
,
Känsäkoski, Johanna
,
Mårtenson, Emma
,
Västinsalo, Hanna
,
Schleit, Jennifer
,
Sankila, Eeva-Marja
,
Kere, Annakarin
,
Junnila, Heidi
,
Siivonen, Pauli
,
Andreevskaya, Margarita
,
Kytölä, Ville
,
Muona, Mikko
,
Salmenperä, Pertteli
,
Myllykangas, Samuel
,
Koskenvuo, Juha
,
Alastalo, Tero-Pekka
Published in
Translational vision science & technology
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Two Finnish USH1B patients with three novel mutations in myosin VIIA
by
Vastinsalo, Hanna
,
Isosomppi, Juha
,
Aittakorpi, Anne
,
Sankila, Eeva-Marja
Published in
Molecular vision
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CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development: e1000607
by
Geller, Scott F
,
Guerin, Karen I
,
Visel, Meike
,
Pham, Aaron
,
Lee, Edwin S
,
Dror, Amiel A
,
Avraham, Karen B
,
Hayashi, Toshinori
,
Ray, Catherine A
,
Reh, Thomas A
,
Bermingham-McDonogh, Olivia
,
Triffo, William J
,
Bao, Shaowen
,
Isosomppi, Juha
,
Västinsalo, Hanna
,
Sankila, Eeva-Marja
,
Flannery, John G
Published in
PLoS genetics
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Molecular Vision
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