ePrints
Items where Author is "Haan, E"
 | Up a level |
Group by: Item Type | No Grouping
Number of items: 2.
Article
Javadiyan, S, Craig, JE, Sharma, S, Lower, KM, Casey, T, Haan, E, Souzeau, E and Burdon, KP 
ORCID: 0000-0001-8217-1249 2017
, 'Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)'
, BMC Medical Genetics, vol. 18, no. 1
, pp. 1-6
, doi: https://doi.org/10.1186/s12881-017-0414-7.
ORCID: 0000-0001-8217-1249 2017
, 'Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)'
, BMC Medical Genetics, vol. 18, no. 1
, pp. 1-6
, doi: https://doi.org/10.1186/s12881-017-0414-7.
Javadiyan, S, Craig, JE, Sharma, Shiwani, Lower, KM, Casey, T, Haan, E, Souzeau, E and Burdon, KP ORCID: 0000-0001-8217-1249 2017
, 'Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)'
, BMC Medical Genetics, vol. 18, no. 1
, pp. 1-6
, doi: https://doi.org/10.1186/s12881-017-0414-7.
ORCID: 0000-0001-8217-1249 2017
, 'Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)'
, BMC Medical Genetics, vol. 18, no. 1
, pp. 1-6
, doi: https://doi.org/10.1186/s12881-017-0414-7.