Erratum: Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications (Osteoporos Int, (2012) 23, 11, (2713-2718), 10.1007/s00198-011-1878-5);Autosomal recessive osteopetrosis: Report of 41 novel mutations in the TCIRG1 gene and diagnostic implications

Osteoporosis International

Volumn 23, Issue 11, 2012, Pages 2713-2718

  Pangrazio, A ^a,b   Caldana, M E ^a,b   Iacono, N L ^a,b   Mantero, S ^b   Vezzoni, P ^a,b   Villa, A ^a,b   Sobacchi, C ^a  

^a Milan Unit   (Italy)

^b HUMANITAS CLINICAL AND RESEARCH CENTER   (Italy)

Author keywords

ARO; Diagnosis; Genomic deletion; Osteopetrosis; TCIRG1

Indexed keywords

ALBERS SCHOENBERG DISEASE; ARTICLE; DISEASE COURSE; DNA SEQUENCE; EXON; GENE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INTRON; MEMBRANE STRUCTURE; OSTEOLYSIS; PATHOGENICITY; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; STOP CODON; TCIRG1 GENE;

EID: 84868206034     PISSN: 0937941X     EISSN: 14332965     Source Type: Journal    
DOI: 10.1007/s00198-012-1933-x     Document Type: Erratum

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