The identification and characterization of the p.G91 deletion in CRYBA1 in a Chinese family with congenital cataracts

Overview of attention for article published in BMC Medical Genomics, September 2019

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Identification and characterization of novel CRYBA1 #mutation https://t.co/QR2YDSCsjA in a #Chinese family with congenital #cataracts #ophthalmology #eyehealth https://t.co/XQamPtbJH8

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