Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Cell

Volumn 78, Issue 2, 1994, Pages 335-342

  Shiang, Rita ^a   Thompson, Leslie M ^a   Zhu, Ya Zhen ^a   Church, Deanna M ^a   Fielder, Thomas J ^a   Bocian, Maureen ^a   Winokur, Sara T ^a   Wasmuth, John J ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR RECEPTOR;

ACHONDROPLASIA; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 4; DWARFISM; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUNTINGTON CHOREA; MEMBRANE POTENTIAL; NUCLEOTIDE METABOLISM; POINT MUTATION; PRIORITY JOURNAL;

EID: 0027964261     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(94)90302-6     Document Type: Article

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