A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephaly

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|167|11|2808-2816

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.11, 2015-11, pp. : 2808-2816

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