Detalles de la búsqueda
1.
Homozygosity mapping coupled with whole-exome sequencing and protein modelling identified a novel missense mutation in GUCY2D in a consanguineous Pakistani family with Leber congenital amaurosis.
J Genet
; 1002021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34470921
Resultados
1 -
1
de 1
1
Próxima >
>>