DMD‐related muscular dystrophy in Cameroon: Clinical and genetic profiles

por Wonkam‐Tingang, Edmond, Nguefack, Séraphin, Esterhuizen, Alina I., Chelo, David, Wonkam, Ambroise
Publicado 2020

Hearing loss in Africa: current genetic profile

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Aboagye, Elvis Twumasi, Quaye, Osbourne, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2021

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

por Aboagye, Elvis Twumasi, Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Amenga-Etego, Lucas, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2023

Knowledge and Challenges Associated With Hearing Impairment in Affected Individuals From Cameroon (Sub-Saharan Africa)

por Wonkam-Tingang, Edmond, Kengne Kamga, Karen, Adadey, Samuel Mawuli, Nguefack, Seraphin, De Kock, Carmen, Munung, Nchangwi Syntia, Wonkam, Ambroise
Publicado 2021

Hearing Impairment Overview in Africa: the Case of Cameroon

por Wonkam Tingang, Edmond, Noubiap, Jean Jacques, F. Fokouo, Jean Valentin, Oluwole, Oluwafemi Gabriel, Nguefack, Séraphin, Chimusa, Emile R., Wonkam, Ambroise
Publicado 2020

Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)

por Kengne Kamga, Karen, Nguefack, Séraphin, Minka, Khuthala, Wonkam Tingang, Edmond, Esterhuizen, Alina, Nchangwi Munung, Syntia, De Vries, Jantina, Wonkam, Ambroise
Publicado 2020

Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Twumasi Aboagye, Elvis, Nayo-Gyan, Daniel Wonder, Boatemaa Ansong, Maame, Quaye, Osbourne, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2020

Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment

por Wonkam-Tingang, Edmond, Schrauwen, Isabelle, Esoh, Kevin K., Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Nasir, Abdul, Adadey, Samuel M., Mowla, Shaheen, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2020

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Alves de Souza Rios, Leonardo, Aboagye, Elvis Twumasi, Esoh, Kevin, Manyisa, Noluthando, De Kock, Carmen, Awandare, Gordon A., Mowla, Shaheen, Wonkam, Ambroise
Publicado 2022

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

por Adadey, Samuel M., Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Bharadwaj, Thashi, Esoh, Kevin K., Basit, Sulman, Acharya, Anushree, Nouel-Saied, Liz M., Liaqat, Khurram, Wonkam-Tingang, Edmond, Mowla, Shaheen, Awandare, Gordon A., Ahmad, Wasim, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2021

A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

por Manyisa, Noluthando, Schrauwen, Isabelle, de Souza Rios, Leonardo Alves, Mowla, Shaheen, Tekendo-Ngongang, Cedrik, Popel, Kalinka, Esoh, Kevin, Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Nasir, Abdul, Wonkam-Tingang, Edmond, de Kock, Carmen, Dandara, Collet, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2021

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

por Wonkam, Ambroise, Adadey, Samuel Mawuli, Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Wonkam-Tingang, Edmond, Esoh, Kevin, Popel, Kalinka, Manyisa, Noluthando, Jonas, Mario, deKock, Carmen, Nembaware, Victoria, Cornejo Sanchez, Diana M., Bharadwaj, Thashi, Nasir, Abdul, Everard, Jenna L., Kadlubowska, Magda K., Nouel-Saied, Liz M., Acharya, Anushree, Quaye, Osbourne, Amedofu, Geoffrey K., Awandare, Gordon A., Leal, Suzanne M.
Publicado 2022