A De Novo Missense Variant in POU3F2 Identified in a Child...

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Neuropediatrics 2018 / 09

A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental Delay

Westphal, Dominik, Riedhammer, Korbinian, Kovacs-Nagy, Reka, Meitinger, Thomas, Hoefele, Julia, Wagner, Matias
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Language:
english
Journal:
Neuropediatrics
DOI:
10.1055/s-0038-1669926
Date:
September, 2018
File:
PDF, 109 KB
english, 2018
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