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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.

Keri M RamseyNewell BelnapAnna BonfittoWayne JepsenMarcus NaymikMeredith Sanchez-CastilloDavid W CraigSzabolcs SzelingerMatthew J HuentelmanVinodh NarayananSampathkumar Rangasamy
Published in: Molecular genetics & genomic medicine (2022)
Keyphrases
  • multiple sclerosis
  • early onset