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RT @NeuroGen_papers: IoN UCL PubMed: Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary sp…
RT @NeuroGen_papers: IoN UCL PubMed: Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary sp…
IoN UCL PubMed: Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia. https://t.co/2kGHxHpaEe
Open Access UCL Research: Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia https://t.co/GowLdcr86y