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Journal description
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Details for article 8 of 11 found articles
| Title: |
Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation |
| Author: |
Buchert, Rebecca Uebe, Steffen Radwan, Farah Tawamie, Hasan Issa, Shaher Shimazaki, Haruo Henneke, Marco Ekici, Arif B. Reis, André Abou Jamra, Rami |
| Appeared in: |
European journal of medical genetics |
| Paging: | Volume 56 (2013) nr. 11 pages 4 p. |
| Year: |
2013 |
| Contents: | |
| Publisher: |
Elsevier Masson SAS |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 8 of 11 found articles
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