학술논문
'학술논문'
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Academic Journal
Powers, Regina M; Daza, Ray; Koehler, Alanna E; Courchet, Julien; Calabrese, Barbara; Hevner, Robert F; Halpain, Shelley
Molecular Biology of the Cell. 33(7)
Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2.
Academic Journal
Macnamara, Ellen F; Koehler, Alanna E; D'Souza, Precilla; Estwick, Tyra; Lee, Paul; Vezina, Gilbert; Undiagnosed Diseases Network; Fauni, Harper; Braddock, Stephen R; Torti, Erin; Holt, James Matthew; Sharma, Prashant; Malicdan, May Christine V; Tifft, Cynthia J
Human mutation. 40(5)
Academic Journal
Friedman, Jennifer; Smith, Desiree E; Issa, Mahmoud Y; Stanley, Valentina; Wang, Rengang; Mendes, Marisa I; Wright, Meredith S; Wigby, Kristen; Hildreth, Amber; Crawford, John R; Koehler, Alanna E; Chowdhury, Shimul; Nahas, Shareef; Zhai, Liting; Xu, Zhiwen; Lo, Wing-Sze; James, Kiely N; Musaev, Damir; Accogli, Andrea; Guerrero, Kether; Tran, Luan T; Omar, Tarek EI; Ben-Omran, Tawfeg; Dimmock, David; Kingsmore, Stephen F; Salomons, Gajja S; Zaki, Maha S; Bernard, Geneviève; Gleeson, Joseph G
Nature communications. 10(1)
Academic Journal
Friedman, Jennifer; Smith, Desiree E; Issa, Mahmoud Y; Stanley, Valentina; Wang, Rengang; Mendes, Marisa I; Wright, Meredith S; Wigby, Kristen; Hildreth, Amber; Crawford, John R; Koehler, Alanna E; Chowdhury, Shimul; Nahas, Shareef; Zhai, Liting; Xu, Zhiwen; Lo, Wing-Sze; James, Kiely N; Musaev, Damir; Accogli, Andrea; Guerrero, Kether; Tran, Luan T; Omar, Tarek EI; Ben-Omran, Tawfeg; Dimmock, David; Kingsmore, Stephen F; Salomons, Gajja S; Zaki, Maha S; Bernard, Geneviève; Gleeson, Joseph G
Nature Communications. 10(1)
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[AR] Koehler, Alanna E
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