A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes.
diterbitkan dalam: American Journal of Medical Genetics
tanggal publikasi: 2010-05-01
bahasa: Inggris
subyek utama: neurodevelopmental disorder, homozygosity
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Artikel - wd:Q51909606