Dr. A.I. den Hollander

Update Persondata

• blindness
• diseases
• genetics
• inherited
• molecular
• multifactorial
• retina

Active as

Publications

(the most recent at the top)

Chromosomal abnormalities resembling Joubert syndrome: two cases illustrating the diagnostic pitfalls

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice

Evaluation of serum lipid concentrations and genetic variants at high-density lipoprotein metabolism loci and TIMP3 in age-related macular degeneration

Identification of novel mutations in pakistani families with autosomal recessive retinitis pigmentosa

CLRN1 mutations cause nonsyndromic retinitis pigmentosa

All publications..

Current research

(the most recent research is at the top)
Project leader	Elucidating and exploiting inhibitory memories to treat drug addiction

Completed research projects

(the most recent research is at the top)
Project leader	Research into the genes for congenital blindness

Classification

D21400	Genetics
D23233	Ophthalmology