GLYCOSIDASES IN SKIN AND PLASMA IN HUNTERS SYNDROME - ABNORMALITY OF A BETA-GALACTOSIDASE IN SKIN

被引:27
作者
OCKERMAN, PA
KOHLIN, P
机构
来源
ACTA PAEDIATRICA SCANDINAVICA | 1968年 / 57卷 / 04期
关键词
D O I
10.1111/j.1651-2227.1968.tb07292.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:281 / &
相关论文
共 9 条
[1]   DIAGNOSIS OF HURLERS SYNDROME IN HOSPITAL LABORATORY AND DETERMINATION OF ITS GENETIC TYPE [J].
MANLEY, G ;
HAWKSWORTH, J .
ARCHIVES OF DISEASE IN CHILDHOOD, 1966, 41 (215) :91-+
[2]   HURLERS DISEASE MORQUIOS DISEASE AND RELATED MUCOPOLYSACCHARIDOSES [J].
MAROTEAUX, P ;
LAMY, M .
JOURNAL OF PEDIATRICS, 1965, 67 (02) :312-+
[3]   GENETIC MUCOPOLYSACCHARIDOSES [J].
MCKUSICK, VA ;
KAPLAN, D ;
WISE, D ;
HANLEY, WB ;
SUDDARTH, SB ;
SEVICK, ME ;
MAUMANEE, AE .
MEDICINE, 1965, 44 (06) :445-+
[4]  
MCKUSICK VA, 1966, HERITABLE DISORDERS
[5]  
OCKERMAN PA, IN PRESS
[6]  
OCKERMAN PA, 1967, 15 SCAND C PAED BERG
[7]  
TELLER WM, 1962, J LAB CLIN MED, V59, P95
[8]  
TERRY K, 1964, P SOC EXP BIOL MED, V115, P394
[9]  
VANHOOF F, 1967, 4 M FED EUR BIOCH SO