

Author: Micheal Shazia Niewold Ilse Therésia Gabriëla Siddiqui Sorath Noorani Zafar Saemah Nuzhat Khan Muhammad Imran Bergen Arthur A. B.
Publisher: MDPI
E-ISSN: 2073-4425|9|2|112-112
ISSN: 2073-4425
Source: Genes, Vol.9, Iss.2, 2018-02, pp. : 112-112
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content




PDGFRB mutation causes autosomal‐dominant Penttinen syndrome
CLINICAL GENETICS, Vol. 88, Iss. 6, 2015-12 ,pp. :




Mutations in SLC6A17 cause autosomal‐recessive intellectual disability
CLINICAL GENETICS, Vol. 88, Iss. 2, 2015-08 ,pp. :


Autosomal recessive primary microcephaly due to ASPM mutations: An update
HUMAN MUTATION, Vol. 39, Iss. 3, 2018-03 ,pp. :