Search Results - Mutaz Amin

The prolactin receptor gene (PRLR) is linked and associated with the risk of polycystic ovarian syndrome by Mutaz Amin, Claudia Gragnoli

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Linkage and association of variants in the dopamine receptor 2 gene (DRD2) with polycystic ovary syndrome by Mutaz Amin, Nicholas Horst, Claudia Gragnoli

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Novel corticotropin-releasing hormone receptor genes (CRHR1 and CRHR2) linkage to and association with polycystic ovary syndrome by Mutaz Amin, Nicholas Horst, Rongling Wu, Claudia Gragnoli

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Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family by Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Mustafa A. M. Salih, Ashraf Yahia, Rayan A. Siddig, Mutaz Amin, Mahmoud Koko, Mustafa I. Elbashir, Muntaser E. Ibrahim, Alexis Brice, Ammar E. Ahmed, Giovanni Stevanin

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A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability by Mutaz Amin, Cedric Vignal, Esraa Eltaraifee, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Arwa Babai, Iman Elbadi, Doua Mustafa, Rayan Abubaker, Mohamed Mustafa, Severine Drunat, Liena E. O. Elsayed, Ammar E. Ahmed, Odile Boespflug-Tanguy, Imen Dorboz

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