Orphanet: Diagn�stico molecular de la sordera neurosensorial no sindr�mica autos�mica dominante, tipo DFNA genes GJB3, MYH14, EYA4, MYO7A, TECTA, COL11A2, MYH9, MYO6, TMC1, MYO1A, GRHL2
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Molecular diagnosis of autosomal dominant nonsyndromic sensorineural deafness type DFNA (GJB3, MYH14, EYA4, MYO7A, TECTA, COL11A2, MYH9, MYO6, TMC1, MYO1A, GRHL2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 20/02/2013
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Last update: February 2013

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of genes tested (including panels) (11)
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