Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. (Q42056628)

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scientific article published on 20 February 2013
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Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum.
scientific article published on 20 February 2013

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    Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum (English)

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