Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.

scientific article published in February 2009

Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/GTMB.2008.0055
P698PubMed publication ID19309273

P2093author name stringVanita Vanita
Jai Rup Singh
Karl Sperling
Hardas Singh Sandhu
Parvinder Singh Sandhu
P433issue1
P921main subjectIndiaQ668
hereditary multiple exostosesQ1952467
P304page(s)43-49
P577publication date2009-02-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleNovel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
P478volume13

Reverse relations

cites work (P2860)
Q52564858A review of skeletal dysplasia research in India.
Q37720019Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing
Q34618180Multiple heriditary exostoses in a family for three generation of Indian origin with review of literature.
Q37709224Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses
Q64264987RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas

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