| Literature DB >> 744199 |
Abstract
A family with Charcot-Marie-Tooth disease (CMT) is described. An irregular dominant sex-linked inheritance is observed. No linkage relationship between the Xg(a) blood group locus and the CMT locus was established. Abnormal values of the serum alkaline phosphatase level were found in affected and unaffected members.Entities:
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Year: 1978 PMID: 744199 DOI: 10.1159/000114972
Source DB: PubMed Journal: Eur Neurol ISSN: 0014-3022 Impact factor: 1.710