A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

Research output: Contribution to journalJournal articleResearchpeer-review

Original languageEnglish
JournalJournal of Human Genetics
Volume61
Issue number3
Pages (from-to)271-273
Number of pages3
ISSN1434-5161
DOIs
Publication statusPublished - Mar 2016

ID: 155607312