Spastic Paraplegia, Optic Atrophy, and Neuropathy (SPOAN): New Observations, Locus Refinement, and Exclusion of Candidate Genes

被引:0
|
作者
Kok, Fernando
Macedo-Souza, Lucia Ines
Silvana, Santos
Amorim, Simone C.
Licinio, Luciana
Graciani, Zodja
Otto, Paulo A.
Zatz, Mayana
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:A393 / A393
页数:1
相关论文
共 32 条
  • [31] Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes
    Ismail, Muhammad
    Abid, Aiysha
    Anwar, Khalid
    Mehdi, S. Qasim
    Khaliq, Shagufta
    JOURNAL OF HUMAN GENETICS, 2006, 51 (09) : 827 - 831
  • [32] Refinement of the X-linked Nonsyndromic High-Grade Myopia Locus MYP1 on Xq28 and Exclusion of 13 Known Positional Candidate Genes by Direct Sequencing (vol 52, pg 6814, 2011)
    Ratnamala, Uppala
    Lyle, Robert
    Rawal, Rakesh
    Singh, Raminder
    Vishnupriya, Satti
    Himabindu, Pamini
    Rao, Vittal
    Aggarwal, Somesh
    Paluru, Prasuna
    Bartoloni, Lucia
    Young, Terri L.
    Paoloni-Giacobino, Ariane
    Morris, Michael A.
    Nath, Swapan K.
    Antonarakis, Stylianos E.
    Radhakrishna, Uppala
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2011, 52 (11) : 7909 - 7909