Saima Siddiqi

1PUBLICATIONS
2CO-AUTHORS
Gene mapping
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Publications (1)

|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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