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A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis

Published Online: 2018-03-22

Authors

Ibrahim, M. T.

Alarcon-Martinez, T.

Lopez, I.

Fajardo, N.

Chiang, J.

Koenekoop, R. K.
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Text and Data Mining valid from 2018-03-22

Version of Record valid from 2018-03-22
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Article History

Received: 13 November 2017

Accepted: 27 February 2018

First Online: 22 March 2018

Competing Interests

: The authors declare no competing interests.

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