Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11

被引：35

作者：

De Sandre-Giovannoli, A

Delague, V

Hamadouche, T

Chaouch, M

Krahn, M

Boccaccio, I

Maisonobe, T

Chouery, E

Jabbour, R

Atweh, S

Grid, D

Mégarbané, A

Lévy, N

机构：

[1] Fac Med Timone, INSERM, U491, F-13385 Marseille 05, France

[2] Campus Hosp & Univ Timone, Dept Med Genet, Marseille, France

[3] Ctr Hosp Univ Ben Aknoun, Serv Neurol, Algiers, Algeria

[4] Hop La Pitie Salpetriere, Serv Neuropathol, Paris, France

[5] Univ St Joseph, Fac Med, Unite Genet Med, Beirut, Lebanon

[6] Genethon III, Evry, France

[7] Amer Univ Beirut, Med Ctr, Beirut, Lebanon

来源：

JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷 / 03期

关键词：

D O I：

10.1136/jmg.2004.024364

中图分类号：

Q3 [遗传学];

学科分类号：

071007 [遗传学]; 090102 [作物遗传育种];

摘要：

[No abstract available]

引用

页码：260 / 265

页数：6

共 42 条

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