A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients
Crossref DOI link: https://doi.org/10.1007/8904_2018_107
Published Online: 2018-05-03
Published Print: 2018
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Musa, Sara
Eyaid, Wafaa
Kamer, Kimberli
Ali, Rehab
Al-Mureikhi, Mariam
Shahbeck, Noora
Al Mesaifri, Fatma
Makhseed, Nawal
Mohamed, Zakkiriah
AlShehhi, Wafaa Ali
Mootha, Vamsi K.
Juusola, Jane
Ben-Omran, Tawfeg
Text and Data Mining valid from 2018-01-01