The clinical application of preimplantation genetic diagnosis for X-linked retinitis pigmentosa

[1] Hamel C(2006)Retinitis pigmentosa Orphanet J Rare Dis 1 40-129

[2] Ali MU(2017)Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario 3 Biotech 7 251-114

[3] Rahman MSU(2012)Current mutation discovery approaches in retinitis pigmentosa Vis Res 75 117-41

[4] Cao J(2010)Multiprotein complexes of retinitis pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked retinitis pigmentosa (XLRP) Adv Exp Med Biol 664 105-770

[5] Yuan PX(2015)RPGR: its role in photoreceptor physiology, human disease, and future therapies Exp Eye Res 138 32-2002

[6] Anasagasti A(1990)Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification Nature. 344 768-910

[7] Irigoyen C(2018)Prenatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014 J Assist Reprod Genet 35 1995-15969

[8] Barandika O(2018)Prenatal and preimplantation genetic diagnosis for single gene disorders: a population-based study from 1977 to 2016 Prenat Diagn 38 904-547

[9] López de Munain A(2015)Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses Proc Natl Acad Sci U S A 112 15964-832

[10] Ruiz-Ederra J(2016)Clinical applications of MARSALA for preimplantation genetic diagnosis of spinal muscular atrophy J Genet Genomics 43 541-546

[1] Hamel C(2006)Retinitis pigmentosa Orphanet J Rare Dis 1 40-129

[2] Ali MU(2017)Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario 3 Biotech 7 251-114

[3] Rahman MSU(2012)Current mutation discovery approaches in retinitis pigmentosa Vis Res 75 117-41

[4] Cao J(2010)Multiprotein complexes of retinitis pigmentosa GTPase regulator (RPGR), a ciliary protein mutated in X-linked retinitis pigmentosa (XLRP) Adv Exp Med Biol 664 105-770

[5] Yuan PX(2015)RPGR: its role in photoreceptor physiology, human disease, and future therapies Exp Eye Res 138 32-2002

[6] Anasagasti A(1990)Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification Nature. 344 768-910

[7] Irigoyen C(2018)Prenatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014 J Assist Reprod Genet 35 1995-15969

[8] Barandika O(2018)Prenatal and preimplantation genetic diagnosis for single gene disorders: a population-based study from 1977 to 2016 Prenat Diagn 38 904-547

[9] López de Munain A(2015)Live births after simultaneous avoidance of monogenic diseases and chromosome abnormality by next-generation sequencing with linkage analyses Proc Natl Acad Sci U S A 112 15964-832

[10] Ruiz-Ederra J(2016)Clinical applications of MARSALA for preimplantation genetic diagnosis of spinal muscular atrophy J Genet Genomics 43 541-546