Identification of two novel SH3PXD2B gene mutations in...

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Gene 2017 / 7

Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature

Zrhidri, Abdelali, Jaouad, Imane Cherkaoui, Lyahyai, Jaber, Raymond, Laure, Egéa, Grégory, Taoudi, Mohamed, Mouatassim, Said E.L., Sefiani, Abdelaziz
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Language:
english
Journal:
Gene
DOI:
10.1016/j.gene.2017.07.011
Date:
July, 2017
File:
PDF, 729 KB
english, 2017
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