A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family
Research output: Contribution to journal › Journal article › Research › peer-review
Original language | English |
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Journal | Journal of Human Genetics |
Volume | 61 |
Issue number | 3 |
Pages (from-to) | 271-273 |
Number of pages | 3 |
ISSN | 1434-5161 |
DOIs | |
Publication status | Published - Mar 2016 |
ID: 155607312