Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, PO) gene causes different phenotypes in homozygous and heterozygous carriers within one family

A, Leal; B, Raunstenstrauss; D, Heuss; C, Berghoff; M, Berghoff; G, Del Valle

Year:

2003

Type of Publication:

Article

Journal:

Neurogenetics

Volume:

4

Number:

4

Pages:

191-197

DOI:

https://doi.org/10.1007/s10048-003-0153-0