Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14
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چکیده
منابع مشابه
Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Familial hemiplegic migraine (FHM) is a rare autosomal dominant disorder characterized by episodes of transient hemiparesis followed by headache. Two chromosomal loci are associated to FHM: FHM1 on chromosome 19 and FHM2 on chromosome 1q21-23. Mutations of the alpha-1A subunit of the voltage gated calcium channel (CACNA1A) are responsible for FHM1. FHM2 critical region spans 28 cM, hence hamper...
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ژورنال
عنوان ژورنال: Journal of Medical Genetics
سال: 2005
ISSN: 1468-6244
DOI: 10.1136/jmg.2005.035766