Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa

Lubala K., Tonic; Lumaka Zola, Aimé; Shongo, Mick; Mbuyi-Musanzayi, Sébastien; Ndua-Musole, M.; Mukuku, Olivier; Yogolelo Asani, Bienvenu; Lubala N.; Kayembe-Kitenge, Tony; Lalamba-Lez; uboya; Devriendt, Koenraad; Lukusa-Tshilobo, Prosper

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Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa

Lubala K., Tonic; Lumaka Zola, Aimé; Shongo, Mick et al.

2015 • 2nd Congress of the Congolese Society for Human Genetics

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https://hdl.handle.net/2268/243917

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Disciplines :

Neurology
Laboratory medicine & medical technology
Pediatrics

Author, co-author :

Lubala K., Tonic

Lumaka Zola, Aimé ; Université de Liège - ULiège > Cancer-Human Genetics

Shongo, Mick

Mbuyi-Musanzayi, Sébastien

Ndua-Musole, M.

Mukuku, Olivier

Yogolelo Asani, Bienvenu

Lubala N.

Kayembe-Kitenge, Tony

Lalamba-Lez

More authors (3 more)

Language :

English

Title :

Molecular evidence for full mutations in the FMR1 gene and fragile X syndrome in the Bantu-speaking population in Central Africa

Publication date :

2015

Event name :

2nd Congress of the Congolese Society for Human Genetics

Event organizer :

Congolese Society for Human Genetics

Event place :

Lubumbashi, Congo - Brazzaville

Event date :

May 11-14, 2015

Available on ORBi :

since 22 January 2020

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