TGFA: Exon-intron structure and evaluation as a candidate gene for Alstrom syndrome [1]

Clinical Genetics

Volumn 55, Issue 1, 1999, Pages 61-62

  Collin, G B ^a   Marshall, J D ^a   Naggert, J K ^a   Nishina, P M ^a  

^a JACKSON LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALSTROM SYNDROME; EXON; GENE STRUCTURE; HUMAN; INTRON; LETTER; NEUROPATHY; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; OBESITY; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RETINA DYSTROPHY;

CHROMOSOMES, HUMAN, PAIR 2; DIABETES MELLITUS, TYPE 2; DNA PRIMERS; GENE LIBRARY; HEARING LOSS, SENSORINEURAL; HUMANS; KIDNEY DISEASES; OBESITY; RETINITIS PIGMENTOSA; SYNDROME; TRANSFORMING GROWTH FACTOR ALPHA;

EID: 0032957750     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.550111.x     Document Type: Letter

References (10)