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Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.

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Bibliographic Details
Title: Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series.
Authors: Oh, Jin Kyun1,2 (AUTHOR), Vargas Del Valle, José G.3 (AUTHOR), Lima de Carvalho Jr, Jose Ronaldo1,4,5 (AUTHOR), Sun, Young Joo6 (AUTHOR), Levi, Sarah R.1 (AUTHOR), Ryu, Joseph1 (AUTHOR), Yang, Jing6 (AUTHOR), Nagasaki, Takayuki1 (AUTHOR), Emanuelli, Andres7 (AUTHOR), Rasool, Nailyn8 (AUTHOR), Allikmets, Rando1,9 (AUTHOR), Sparrow, Janet R.1,9 (AUTHOR), Izquierdo, Natalio J.10 (AUTHOR), Duncan, Jacque L.8 (AUTHOR), Mahajan, Vinit B.6,11 (AUTHOR), Tsang, Stephen H.1,9,12 (AUTHOR) sht2@cumc.columbia.edu, Lima de Carvalho, Jose Ronaldo Jr1,4,5 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 4/1/2022, Vol. 17 Issue 1, p1-10. 10p.
Database: Academic Search Ultimate
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Description
ISSN:17501172
DOI:10.1186/s13023-022-02295-9