A novel deep intronic variant in ATP7B...

Molecular Genetics & Genomic Medicine 2020 / 08

A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease

Woimant, France, Poujois, Aurelia, Bloch, Adrien, Jordi, Tabaras, Laplanche, Jean‐Louis, Morel, Hélène, Collet, Corinne
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Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.1428
Date:
August, 2020
File:
PDF, 1.04 MB
2020
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