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Volumn 83, Issue 6, 2013, Pages 527-529
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Opsismodysplasia: Implications of mutations in the developmental gene INPPL1
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Author keywords
[No Author keywords available]
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Indexed keywords
INOSITOL POLYPHOSPHATE;
INSULIN RECEPTOR SUBSTRATE;
PHOSPHATIDYLINOSITOL 3 KINASE;
AUTOSOMAL RECESSIVE INHERITANCE;
BONE DYSPLASIA;
CONSANGUINEOUS MARRIAGE;
FRAMESHIFT MUTATION;
GENE;
GENE EXPRESSION;
GENE MUTATION;
GENOTYPE;
GLUCOSE HOMEOSTASIS;
HETEROZYGOSITY;
HISTOPATHOLOGY;
HOMOZYGOSITY;
HUMAN;
INDEL MUTATION;
INPPL1 GENE;
MISSENSE MUTATION;
NONHUMAN;
NONSENSE MUTATION;
NOTE;
OPSISMODYSPLASIA;
OSSIFICATION;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
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EID: 84876801360
PISSN: 00099163
EISSN: 13990004
Source Type: Journal
DOI: 10.1111/cge.12136 Document Type: Note |
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Times cited : (5)
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References (0)
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