CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh, C Rother… - Human …, 2017 - Wiley Online Library
Achromatopsia is a rare autosomal recessive cone disorder characterized by color vision
defects, photophobia, nystagmus, and severely reduced visual acuity. The disease is …
被引用次数：63 相关文章

[引用][C] CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh… - Human …, 2017 - tobias-lib.ub.uni-tuebingen.de
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients …
[PDF] researchgate.net

[PDF][PDF] CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh, C Rother, B Baumann… - researchgate.net
Achromatopsia is a rare autosomal recessive cone disorder characterized by color vision
defects, photophobia, nystagmus, and severely reduced visual acuity. The disease is …

CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients.

AK Mayer, C Van Cauwenbergh, C Rother… - Human …, 2017 - europepmc.org
Achromatopsia is a rare autosomal recessive cone disorder characterized by color vision
defects, photophobia, nystagmus, and severely reduced visual acuity. The disease is …

CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh, C Rother… - Human …, 2017 - pubmed.ncbi.nlm.nih.gov
Achromatopsia is a rare autosomal recessive cone disorder characterized by color vision
defects, photophobia, nystagmus, and severely reduced visual acuity. The disease is …

CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh, C Rother… - HUMAN …, 2017 - biblio.ugent.be
Achromatopsia is a rare autosomal recessive cone disorder characterized by color vision
defects, photophobia, nystagmus, and severely reduced visual acuity. The disease is …

[引用][C] CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

AK Mayer, C Van Cauwenbergh, C Rother… - Human …, 2017 - ub01.uni-tuebingen.de
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients
CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients …