Reversion SAMD9 Mutations Modifying Phenotypic Expression...

Frontiers in Endocrinology 2019 / 9 Vol. 10

Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder

Roucher-Boulez, Florence, Mallet, Delphine, Chatron, Nicolas, Dijoud, Frédérique, Gorduza, Daniela Brindusa, Bretones, Patricia, Morel, Yves
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Volume:
10
Language:
english
Journal:
Frontiers in Endocrinology
DOI:
10.3389/fendo.2019.00625
Date:
September, 2019
File:
PDF, 1.79 MB
english, 2019
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