Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients.

Meins, M

Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients. [electronic resource] - Neuropediatrics Aug 2002 - 194-8 p. digital

Publication Type: Case Reports; Journal Article

0174-304X

10.1055/s-2002-34495 doi


Alexander Disease--genetics
Child
Child, Preschool
DNA Mutational Analysis
Glial Fibrillary Acidic Protein--genetics
Humans
Infant
Infant, Newborn
Male
Mutation--genetics
Prognosis
Twins, Monozygotic--genetics