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UnknownThe MitCHAP-60 disease is due to entropic destabilization of the human mitochondrial Hsp60 oligomer.
Not available
S-EPMC2788871 | biostudies-literature
UnknownA missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred.
Not available
S-EPMC3925280 | biostudies-literature
UnknownOffspring gender ratio and the rate of recurrent spontaneous miscarriages in jewish women at high risk for breast/ovarian cancer.
Not available
S-EPMC1182091 | biostudies-literature
UnknownA single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers.
Not available
S-EPMC30636 | biostudies-literature
UnknownLatitudinal Clines of the Human Vitamin D Receptor and Skin Color Genes.
Not available
S-EPMC4856077 | biostudies-literature
UnknownA nonsense mutation in the human homolog of Drosophila rogdi causes Kohlschutter-Tonz syndrome.
Not available
S-EPMC3322231 | biostudies-literature
UnknownOverall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers.
Not available
S-EPMC4453851 | biostudies-literature
UnknownHereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.
Not available
S-EPMC1380229 | biostudies-literature
UnknownMitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.
Not available
S-EPMC2443844 | biostudies-literature
UnknownHaplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations.
Not available
S-EPMC3548269 | biostudies-literature
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