0000000000213077

AUTHOR

Carrera P

First italian case with a de novo T666M mutation in the CACNA1A gene associated with hemiplegic migraine/progressive cerebellar and episodic ataxia

research product

FIRST ITALIAN CASE WITH A DE NOVO 7666M MUTATION IN THE CACNA1A GENE ASSOCIATED WITH HEMIPLEGIC MIGRAINE/PROGRESSIVE CEREBELLAR AND EPISODIC ATAXIA

research product