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Gene Information

Gene symbol: MPFD

Gene name: myopathy with fiber type disproportion

HGNC ID: 7210

Related Genes

#	Gene Symbol	Number of hits
1	INS	1 hits
2	INSR	1 hits

Related Sentences

#	PMID	Sentence
1	7706500	We report the findings of altered insulin secretion and insulin action in two brothers affected with CFTDM and glucose intolerance as well as in their nonconsanguineous glucose-tolerant parents.
2	7706500	Despite a 45-90-fold increase in both fasting and postprandial serum insulin levels, both CFTDM patients had diabetes mellitus.
3	7706500	In conclusion, CFTDM is a novel form of severe hyperinsulinemia and insulin resistance.
4	7706500	We report the findings of altered insulin secretion and insulin action in two brothers affected with CFTDM and glucose intolerance as well as in their nonconsanguineous glucose-tolerant parents.
5	7706500	Despite a 45-90-fold increase in both fasting and postprandial serum insulin levels, both CFTDM patients had diabetes mellitus.
6	7706500	In conclusion, CFTDM is a novel form of severe hyperinsulinemia and insulin resistance.
7	7706500	We report the findings of altered insulin secretion and insulin action in two brothers affected with CFTDM and glucose intolerance as well as in their nonconsanguineous glucose-tolerant parents.
8	7706500	Despite a 45-90-fold increase in both fasting and postprandial serum insulin levels, both CFTDM patients had diabetes mellitus.
9	7706500	In conclusion, CFTDM is a novel form of severe hyperinsulinemia and insulin resistance.
10	10844410	The insulin receptor (IR) in two brothers with a rare syndrome of congenital muscle fiber type disproportion myopathy (CFTDM) associated with diabetes and severe insulin resistance was studied.
11	10844410	A third brother who inherited both normal alleles has an normal muscle phenotype and insulin sensitivity, suggesting a direct linkage of these IR mutations with the CFTDM phenotype.
12	10844410	The insulin receptor (IR) in two brothers with a rare syndrome of congenital muscle fiber type disproportion myopathy (CFTDM) associated with diabetes and severe insulin resistance was studied.
13	10844410	A third brother who inherited both normal alleles has an normal muscle phenotype and insulin sensitivity, suggesting a direct linkage of these IR mutations with the CFTDM phenotype.