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Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients

Published Online: 2021-04-19

Authors

Laššuthová, P.

Mazanec, R.

Staněk, D.

Sedláčková, L.

Plevová, B.

Haberlová, J.

Seeman, P.
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Text and Data Mining valid from 2021-04-19

Version of Record valid from 2021-04-19
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Article History

Received: 15 January 2021

Accepted: 22 March 2021

First Online: 19 April 2021

Competing interests

: The authors declare no competing interests.

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