Publication | Closed Access
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome
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References
2001
Year
Human 22Q11.2Neurodegenerative DiseasesMolecular NeuroscienceDevelopmental BiologyDigeorge SyndromeGenetic DisorderMendelian DisorderGeneticsDegenerative DiseaseNeurologyMolecular NeurobiologyNeuropathologyMedicineNeurogenetics
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