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Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Médicale UCL
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Gent
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Antwerpen
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - Erasme ULB
Huntington disease - HTT gene CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Brussel VUB
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - CHU Sart-Tilman
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Menselijke Erfelijkheid - KUL
Amyotrophic Lateral Sclerosis (ALS) (gene panel)
Amyotrophic Lateral Sclerosis (ALS) - UGent
Amyotrophic lateral sclerosis
,
Juvenile amyotrophic lateral sclerosis
,
Amyotrophic lateral sclerosis type 4
Centrum Medische Genetica - UZ Gent
Transthyretine amyloïdose
TTR
ATTRV30M amyloidosis
,
ATTRV122I amyloidosis
Centrum Medische Genetica - UZ Gent
Amyloidosis (TTR full sanger exon sequencing)
TTR
Hereditary ATTR amyloidosis
,
ATTRV30M amyloidosis
,
ATTRV122I amyloidosis
Centre de Génétique Humaine - CHU Sart-Tilman
Amyloidosis hereditary / Dystransthyretinemic hyperthyroxinemia
TTR
ATTRV30M amyloidosis
,
ATTRV122I amyloidosis
,
Hereditary ATTR amyloidosis
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Amyloidosis (full sanger screening of the 4 exons for TTR)
TTR
ATTRV30M amyloidosis
,
ATTRV122I amyloidosis
Centrum Menselijke Erfelijkheid - KUL
Hyperparathyroidism (gene panel)
AIP
,
MEN1
,
CDKN1B
,
PRKAR1A
,
RET
Familial isolated hyperparathyroidism
Centre de Génétique Humaine - CHU Sart-Tilman
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