Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A

Authors:	Rivolta Carlo Berson Eliot L Dryja Thaddeus P

Affiliation:	Massachusetts Eye and Ear Infirmary, 243 Charles St, Boston, MA 02114, USA. thaddeus_dryja@meei.harvard.edu

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