A unique form of autosomal dominant cataract explained by gene conversion between β-crystallin B2 and its pseudogene

被引：94

作者：

Vanita

Sarhadi, V

Reis, A

Jung, M

Singh, D

Sperling, K

Singh, JR

Bürger, J

机构：

[1] Humboldt Univ, Charite, Inst Humangenet, D-13353 Berlin, Germany

[2] Guru Nanak Dev Univ, Ctr Genet Disorders, Amritsar, Punjab, India

[3] Max Delbruck Ctr Mol Med, Gene Mapping Ctr, Berlin, Germany

[4] Dr Daljit Singh Eye Hosp, Amritsar, Punjab, India

来源：

JOURNAL OF MEDICAL GENETICS | 2001年 / 38卷 / 06期

关键词：

D O I：

10.1136/jmg.38.6.392

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：392 / 396

页数：5

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