Allan-Herndon-Dudley syndrome: Should the locus for this hereditary spastic paraplegia be designated SPG 22?

被引：7

作者：

Bohan, TP ^{[1
]}

Azizi, P ^{[1
]}

机构：

[1] Baylor Coll Med, Texas Childrens Hosp, Dept Pediat, Meyer Ctr Dev Pediat, Houston, TX 77030 USA

来源：

ARCHIVES OF NEUROLOGY | 2004年 / 61卷 / 09期

关键词：

D O I：

10.1001/archneur.61.9.1470-c

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：1470 / 1471

页数：2

共 7 条

[1]

Allan W, 1944, AM J MENT DEF, V48, P325

[2] ALLAN-HERNDON-DUDLEY SYNDROME - CLINICAL AND LINKAGE STUDIES ON A 2ND FAMILY [J].

BIALER, MG ;

LAWRENCE, L ;

STEVENSON, RE ;

SILVERBERG, G ;

WILLIAMS, MK ;

ARENA, JF ;

LUBS, HA ;

SCHWARTZ, CE .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (1-2) :491-497

[3]

BUNDEY S, 1991, AM J HUM GENET, V48, P1214

[4]

Claes S, 2000, AM J MED GENET, V94, P1, DOI 10.1002/1096-8628(20000904)94:1<1::AID-AJMG1>3.0.CO

[5]

2-V

[6] The hereditary spastic paraplegias - Nine genes and counting [J].

Fink, JK .

ARCHIVES OF NEUROLOGY, 2003, 60 (08) :1045-1049

[7] Further evidence for a fourth gene causing X-linked pure spastic paraplegia [J].

Starling, A ;

Rocco, P ;

Cambi, F ;

Hobson, GM ;

Bueno, MRP ;

Zatz, M .

AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 111 (02) :152-156

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