Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

被引：9

作者：

Beckmann, JS

Richard, I

Broux, O

Fougerousse, F

Allamand, V

Chiannilkulchai, N

Lim, LE

Duclos, F

Bourg, N

Brenguier, L

Pasturaud, P

Quetier, F

Roudaut, C

Sunada, Y

Meyer, J

Dincer, P

Lefranc, G

Merlini, L

Topaloglu, H

Tome, FMS

Cohen, D

Jackson, CE

Campbell, KP

Fardeau, M

机构：

[1] UNIV IOWA, HOWARD HUGHES MED INST, IOWA CITY, IA 52242 USA

[2] HACETTEPE UNIV, ANKARA, TURKEY

[3] UMR CNRS 9942, MONTPELLIER, FRANCE

[4] INST ORTOPED RIZZOLI, BOLOGNA, ITALY

[5] INSERM U153, PARIS, FRANCE

[6] FDN JEAN DAUSSET, CEPH, PARIS, FRANCE

[7] HENRY FORD HOSP, DETROIT, MI 48202 USA

来源：

NEUROMUSCULAR DISORDERS | 1996年 / 6卷 / 06期

关键词：

limb girdle muscular dystrophy; LGMD; positional cloning;

D O I：

10.1016/S0960-8966(96)00386-0

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The autosomal recessive forms of limb-girdle muscular dystrophies are encoded by at least five distinct genes. The work performed towards the identification of two of these is summarized in this report. This success illustrates the growing importance of genetics in modern nosology.

引用

收藏

页码：455 / 462

页数：8

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