%0
Generic
%T
A further case of AFG2B‐related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313TC, p.(Leu438Pro)
%A Grosch, Sarah
%A Kehrer, Martin
%A Riess, Olaf
%A Bevot, Andrea
%A Haack, Tobias B.
%I Wiley
%@ 2324-9269
%K Genetics (clinical)
%K Genetics
%K Molecular Biology
%D 2024
%C Wiley
%U http://slubdd.de/katalog?TN_libero_mab2