IDENTIFICATION OF A DE-NOVO INSERTIONAL MUTATION IN P-O IN A PATIENT WITH A DEJERINE-SOTTAS SYNDROME (DSS) PHENOTYPE

被引：53

作者：

RAUTENSTRAUSS, B

NELIS, E

GREHL, H

PFEIFFER, RA

VAN BROECKHOVEN, C

机构：

[1] UNIV ANTWERP, BORN BUNGE FDN, DEPT BIOCHEM, NEUROGENET LAB, B-2610 ANTWERP, BELGIUM

[2] UNIV ERLANGEN NURNBERG, INST HUMAN GENET, D-91054 ERLANGEN, GERMANY

[3] UNIV ERLANGEN NURNBERG, DEPT NEUROL, D-91054 ERLANGEN, GERMANY

来源：

HUMAN MOLECULAR GENETICS | 1994年 / 3卷 / 09期

关键词：

D O I：

10.1093/hmg/3.9.1701

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：1701 / 1702

页数：2

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