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Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36

✍ Scribed by Al-Qattan, Mohammad M.; Shamseldin, Hanan E.; Al Mazyad, Mohammed; Al Deghaither, Saud; Alkuraya, Fowzan S.


Book ID
120363363
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
249 KB
Volume
161
Category
Article
ISSN
1552-4825

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Familial hypobetalipoproteinemia (FHBL) is an autosomal dominant disorder of lipid metabolism characterized by extremely low plasma levels of apolipoprotein B (apoB), and total-, and low-density lipoprotein (LDL) cholesterol. Various truncated forms of apoB have been found to cosegregate with the FH