Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases

Gene

Volumn 392, Issue 1-2, 2007, Pages 142-150

  Peng, Jianbin ^a   Redman, Colvin M ^a   Wu, Xu ^a   Song, Xiaoling ^a   Walker, Ruth H ^b   Westhoff, Connie M ^c   Lee, Soohee ^a  

^a NEW YORK BLOOD CENTER   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c AMERICAN RED CROSS   (United States)

Author keywords

Adaptive evolution; Chronic granulomatous disease; Duchenne muscular dystrophy; Ornithine transcarbamylase deficiency; Retinitis pigmentosa; X linked disorders

Indexed keywords

ADULT; ARTICLE; BASE PAIRING; CASE REPORT; CHROMOSOME XP; CHRONIC GRANULOMATOUS DISEASE; CONTROLLED STUDY; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; DUCHENNE MUSCULAR DYSTROPHY; GENE DELETION; GENE LOCUS; GENETIC SELECTION; HUMAN; HUMAN CELL; HYPERTRANSLUCENT LUNG; MALE; PHENOTYPE; PHYLOGENY; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SUBSTITUTION REACTION; X CHROMOSOME LINKED DISORDER;

ACANTHOCYTES; AMINO ACID TRANSPORT SYSTEMS, NEUTRAL; BASE SEQUENCE; BLOOD GROUP ANTIGENS; CHROMOSOME MAPPING; FEMALE; GENE DELETION; HUMANS; INFANT; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; NEUROMUSCULAR DISEASES; PHENOTYPE; SYNDROME;

AVES; MAMMALIA;

EID: 33947608938     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gene.2006.11.023     Document Type: Article

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