Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS)

Genomics

Volumn 34, Issue 2, 1996, Pages 166-172

  Schaefer, L ^a   Ballabio, A ^a   Zoghbi, H Y ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HOLOCYTOCHROME C TYPE SYNTHETASE; PEPTIDE SYNTHASE; UNCLASSIFIED DRUG;

ARTICLE; EMBRYO; ENZYME ISOLATION; GENE EXPRESSION REGULATION; GENE ISOLATION; GENE MAPPING; HUMAN; HUMAN CELL; MICROPHTHALMIA; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; X CHROMOSOMAL INHERITANCE;

MAMMALIA; MURINAE;

EID: 0029882297     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0261     Document Type: Article

References (0)