One disease with two faces: Semidominant inheritance of a novel HTRA1 mutation in a consanguineous family
CE Bekircan-Kurt, A Çetinkaya, R Gocmen… - Journal of Stroke and …, 2021 - Elsevier
Objectives To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family.
CE Bekircan-Kurt, A Çetinkaya, R Gocmen… - Journal of Stroke and …, 2021 - europepmc.org
Objectives To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family
CAN Bekircan-Kurt, A ÇETİNKAYA… - … OF STROKE & …, 2021 - avesis.hacettepe.edu.tr
Objectives: To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family
CE Bekircan-Kurt, A Çetinkaya… - Journal of stroke …, 2021 - pubmed.ncbi.nlm.nih.gov
Objectives To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family
CE Bekircan-Kurt, A Çetinkaya, R Gocmen… - Journal of Stroke and …, 2021 - strokejournal.org
Objectives To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …
One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family
CE Bekircan-Kurt, A Çetinkaya, R Gocmen… - Journal of Stroke and …, 2021 - strokejournal.org
Objectives To identify the underlying genetic defect for a consanguineous family with an
unusually high number of members affected by cerebral small vessel disease. Materials and …
unusually high number of members affected by cerebral small vessel disease. Materials and …