A Novel GJC2 Mutation Associated with Hypomyelination and Mullerian Agenesis Syndrome: Coincidence or a New Entity?

C. Yalcinkaya, O. Erturk, B. Tuysuz, G. Yesil, J.I.M.L. Verbeke, B. Keyser, M. Stuhrmann, D. Steinemann, E.A. Sistermans, M.S. van der Knaap

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)159-161
JournalNeuropediatrics
Volume43
Issue number3
DOIs
Publication statusPublished - 2012

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