The autosomal recessive form of CMT disease linked to 5q31-q33

被引：3

作者：

Guilbot, A

Kessali, M

Ravisé, N

Hammadouche, T

Bouhouche, A

Maisonobe, T

Grid, D

Brice, A

LeGuern, E

机构：

[1] Hop La Pitie Salpetriere, INSERM, U289, F-75651 Paris 13, France

[2] Hop La Pitie Salpetriere, Federat Neurol, F-75651 Paris 13, France

[3] Hop La Pitie Salpetriere, Lab Neuropathol R Escourolle, F-75651 Paris 13, France

[4] Inst Pasteur, Algiers, Algeria

[5] CHU Mustapha, Serv Neurol, Algiers, Algeria

[6] Hop Specialites, Serv Neurol, Rabat, Morocco

来源：

CHARCOT-MARIE-TOOTH DISORDERS | 1999年 / 883卷

关键词：

D O I：

10.1111/j.1749-6632.1999.tb08608.x

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：453 / 456

页数：4

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