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A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report https://t.co/AUktUJuwhW #bmcneurol
A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report https://t.co/AUktUJuwhW #bmcneurol
RT @NeuroGen_papers: PubMed: A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and… https:/…
PubMed: A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and… https://t.co/aFjo7fWBKA