Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity.

International journal of molecular medicine

Volumn 7, Issue 2, 2001, Pages 155-161

  Pusch, C M ^a   Maurer, J ^a   Ramser, J ^a   Tomiuk, J ^a   Achatz, H ^a   Pesch, K ^a   Lichtner, P ^a   Apfelstedt Sylla, E ^a   Jacobi, F K ^a   Berger, W ^a   Meindl, A ^a   Wissinger, B ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN KINASE (CALCIUM,CALMODULIN); PROTEINASE; UBIQUITIN NALPHA PROTEIN HYDROLASE; UBIQUITIN-NALPHA-PROTEIN HYDROLASE;

ARTICLE; CHROMOSOME MAP; EUROPE; FEMALE; GENETIC LINKAGE; GENETICS; HAPLOTYPE; HUMAN; MALE; NIGHT BLINDNESS; PEDIGREE; X CHROMOSOME;

CA(2+)-CALMODULIN DEPENDENT PROTEIN KINASE; CHROMOSOME MAPPING; ENDOPEPTIDASES; EUROPE; FEMALE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; NIGHT BLINDNESS; PEDIGREE; X CHROMOSOME;

MLCS; MLOWN;

EID: 0035258848     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.7.2.155     Document Type: Article

References (0)