PMP22 related congenital hypomyelination neuropathy.

Fabrizi, G M

PMP22 related congenital hypomyelination neuropathy. [electronic resource] - Journal of neurology, neurosurgery, and psychiatry Jan 2001 - 123-6 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0022-3050

10.1136/jnnp.70.1.123 doi


Adolescent
Demyelinating Diseases--genetics
Female
Humans
Myelin Proteins--genetics
Point Mutation--genetics
Sural Nerve--pathology