Mutations in C10orf11, Encoding a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism
Page 1 of 1
Mutations in C10orf11, Encoding a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism
Grønskov K, Dooley CM, Ostergaard E, Kelsh RN, Hansen L, Levesque MP, Vilhelmsen K, Møllgård K, Stemple DL, Rosenberg T. Mutations in C10orf11, Encoding a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism. Am J Hum Genet. 2013 Feb 5. doi:pii: S0002-9297(13)00037-2. 10.1016/j.ajhg.2013.01.006. [Epub ahead of print]
Last edited by Jon Moulton on Tue Feb 12, 2013 9:28 am; edited 1 time in total (Reason for editing : fix link)
Similar topics
» Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism
» Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism
» Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
» Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
» Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism
» Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
» Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy
» Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum