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
Language | Label | Description | Also known as |
---|---|---|---|
English | Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum. |
scientific article published on 20 February 2013 |
Statements
Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum (English)
A O Caglayan
H Per
H Gumus
J Baranoski
M Canpolat
M Calik
A Yikilmaz
K Bilguvar
S Kumandas
20 February 2013