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

Authors :
Gunel, M.
PER, HÜSEYİN
Akgumus, G.
GÜMÜŞ, HAKAN
Baranoski, J.
CANPOLAT, MEHMET
ÇALIK, MUHAMMED ALPARSLAN
Yikilmaz, A.
Bilguvar, K.
Kumandas, S.
ÇAĞLAYAN, AHMET OKAY
Publication Year :
2013

Subjects

Subjects :
Article

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.pmid.dedup....2de0e9308580ad5fc5c0e806ffaa1eb2

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