ArticleAmerican journal of human genetics2003

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.

H Azzedine et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.