A new NBIA patient from Turkey with homozygous C19ORF12 mutation.


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Kasapkara Ç. S., TÜMER L., Gregory A., Ezgu F. S., İNCİ A., Derinkuyu B. E., ...Daha Fazla

Acta neurologica Belgica, cilt.119, sa.4, ss.623-625, 2019 (SCI-Expanded, Scopus) identifier identifier identifier