A LARGE FAMILY OF VALAIS AFFECTED WITH PROGRESSIVE MYOCLONIC EPILEPSY AND WITH RETINITIS PIGMENTOSA - CLINICAL GENETIC AND ANATOMO-PATHOLOGICAL STUDY

被引：9

作者：

KLEIN, D

MUMENTHALER, M

KRAUSRUP.R

RALLO, E

机构：

来源：

HUMANGENETIK | 1968年 / 6卷 / 03期

关键词：

D O I：

10.1007/BF00291867

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：237 / +

页数：1

共 28 条

[1] ALABASTRO A, 1947, RIV OTONEUROOFTAL, V22, P389
[2] BAMATTER F, 18 C ASS PED LANG FR, V2, P1
[3] BECKER PE, HUMANGENETIK ED, V5, P150
[4] DIEBOLD K, 1967, DTSCH Z NERVENHEILK, V190, P199
[5] FRANCESCHETTI A, HEREDODEGENERESCENCE, V2, P1035
[6] FRANCESCHETTI A, 1948, REV OTONEUROOPHTAL, V20, P109
[7] HALLIDAY AM, MODERN TRENDS NEUROL, V4, P69
[8] HARENKO A, 1961, ACTA NEUROL SCAND, V37, P282
[9] PROGRESSIVE FAMILIAL MYOCLONIC EPILEPSY IN 3 FAMILIES - ITS CLINICAL FEATURES AND PATHOLOGICAL BASIS
HARRIMAN, DGF
MILLAR, JHD
[J]. BRAIN, 1955, 78 (03) : 325 - +
[10] Two cases of patamyoclonus multiplex with epilepsy
Hartung, E
[J]. ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1920, 56 : 150 - 153