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PDF) Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants
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PDF) Genetic evaluation of patients with congenital heart disease
PDF) Regulation of Oligodendrocyte Development and Myelination by Glucose and Lactate
PDF) Genetic evaluation of patients with congenital heart disease
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Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome - Cordeddu - 2015 - Human Mutation - Wiley Online Library
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PDF) Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants
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PDF) Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C
PDF) Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C
Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome - Cordeddu - 2015 - Human Mutation - Wiley Online Library
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PDF) Regulation of Oligodendrocyte Development and Myelination by Glucose and Lactate
PDF) Regulation of Oligodendrocyte Development and Myelination by Glucose and Lactate
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PDF) Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants
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PDF) Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C
