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Identification of a risk transcriptome and proteome in Parkinson's disease, Dementia with Lewy bodies and rapidly progressive
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion - Ullah - 2022 - International Journal of Developmental Neuroscience ...
Identification of a risk transcriptome and proteome in Parkinson's disease, Dementia with Lewy bodies and rapidly progressive
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Identification of a risk transcriptome and proteome in Parkinson's disease, Dementia with Lewy bodies and rapidly progressive
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion - Ullah - 2022 - International Journal of Developmental Neuroscience ...
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Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion - Ullah - 2022 - International Journal of Developmental Neuroscience ...
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