Associated Papers
Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defects.
Yang P et al.
Clinical Genetics, 2021
A novel TUBB4A mutation G96R identified in a patient with hypomyelinating leukodystrophy onset beyond adolescence.
Lu Y et al.
Human Genome Variation, 2017
28791129 (PubMed )
Supplement: hgv201735-s2.pdf
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