Etiology
mutations in MYO5A, which codes for an actin-based molecular motor.
Elejalde disease
Elejalde syndrome is a condition characterized by mild hypopigmentation and severe, primary neurological abnormalities.
Elejalde syndrome is a condition characterized by mild hypopigmentation and severe, primary neurological abnormalities.
Etiology
mutations in MYO5A, which codes for an actin-based molecular motor.