TY -
GEN
AU - Grosch, Sarah
AU - Kehrer, Martin
AU - Riess, Olaf
AU - Bevot, Andrea
AU - Haack, Tobias B.
TI -
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)
PB - Wiley
SN - 2324-9269
KW - Genetics (clinical)
KW - Genetics
KW - Molecular Biology
PY - 2024
UR - http://slubdd.de/katalog?TN_libero_mab2
ER -