Saima Siddiqi
1PUBLICATIONS
2CO-AUTHORS

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Publications (1)
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|Jan 10, 2017
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy.Celia Zazo Seco, Anna Castells-Nobau, Seol-Hee Joo
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