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Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11.
JAMA Ophthalmol. 2015 Jun;133(6):720-1. doi: 10.1001/jamaophthalmol.2015.199.
JAMA Ophthalmol. 2015.
PMID: 25764055
No abstract available.
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness.
Wiley LA, Burnight ER, DeLuca AP, Anfinson KR, Cranston CM, Kaalberg EE, Penticoff JA, Affatigato LM, Mullins RF, Stone EM, Tucker BA.
Wiley LA, et al. Among authors: penticoff ja.
Sci Rep. 2016 Jul 29;6:30742. doi: 10.1038/srep30742.
Sci Rep. 2016.
PMID: 27471043
Free PMC article.
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