A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report
Cherkaoui Jaouad, Imane, Zrhidri, Abdelali, Jdioui, Wafaa, Lyahyai, Jaber, Raymond, Laure, Egéa, Grégory, Taoudi, Mohamed, El Mouatassim, Said, Sefiani, AbdelazizVolume:
19
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-018-0625-6
Date:
December, 2018
File:
PDF, 728 KB
english, 2018