|
|
Volumn 49, Issue 1, 2001, Pages 121-124
|
|
Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families
a
b
c
c
a,b
d
e
e
f
e
a,b
a,g
e
Gesundheitsamt
*
(Germany)
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
DOPAMINE 2 RECEPTOR;
ADOLESCENT;
ADULT;
ARTICLE;
AUTOSOMAL DOMINANT INHERITANCE;
CHILD;
CHROMOSOME 7Q;
CLINICAL ARTICLE;
DNA SEQUENCE;
DYSTONIA;
FEMALE;
GENE LOCUS;
GENE MUTATION;
GENETIC LINKAGE;
GERMANY;
HUMAN;
MALE;
MYOCLONUS;
ONSET AGE;
PRIORITY JOURNAL;
RECEPTOR GENE;
ADOLESCENT;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 7;
DYSTONIA;
FEMALE;
GENOTYPE;
GERMANY;
HUMANS;
LINKAGE (GENETICS);
MALE;
MYOCLONUS;
PEDIGREE;
PHENOTYPE;
SYNDROME;
|
|
EID: 0035112509
PISSN: 03645134
EISSN: None
Source Type: Journal
DOI: 10.1002/1531-8249(200101)49:1<121::AID-ANA20>3.0.CO;2-8 Document Type: Article |
|
Times cited : (40)
|
|
References (8)
|
