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Volumn 13, Issue 4, 1996, Pages 395-396
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Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome
a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
ENDOTHELIN 3;
ENDOTHELIN B RECEPTOR;
PROTEIN TYROSINE KINASE;
CONTROLLED STUDY;
FRAMESHIFT MUTATION;
HIRSCHSPRUNG DISEASE;
HUMAN;
HYPOVENTILATION;
LETTER;
MAJOR CLINICAL STUDY;
PHENOTYPE;
PRIORITY JOURNAL;
SINGLE STRAND CONFORMATION POLYMORPHISM;
SYNDROME;
BASE SEQUENCE;
DNA PRIMERS;
ENDOTHELINS;
FRAMESHIFT MUTATION;
HIRSCHSPRUNG DISEASE;
HUMANS;
HYPOVENTILATION;
MOLECULAR SEQUENCE DATA;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
SYNDROME;
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EID: 0030017530
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/ng0896-395 Document Type: Letter |
Times cited : (86)
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References (0)
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