A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease.

Human mutation

Volumn 17, Issue 2, 2001, Pages 152-

  Hobson, G ^a   Stabley, D ^a   Funanage, V ^a   Marks, H ^a  

^a NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ENDODEOXYRIBONUCLEASE ACYI; PROTEOLIPID PROTEIN; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

ARTICLE; GENETIC POLYMORPHISM; GENETICS; HETEROZYGOTE DETECTION; HUMAN; METABOLISM; PATHOLOGY; PELIZAEUS MERZBACHER DISEASE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

DEOXYRIBONUCLEASE HPAII; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA; HETEROZYGOTE DETECTION; HUMANS; MYELIN PROTEOLIPID PROTEIN; PELIZAEUS-MERZBACHER DISEASE; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0035256449     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200102)17:2<152::AID-HUMU9>3.0.CO;2-P     Document Type: Article

References (0)