Page last updated: 2024-08-17

histidine and Dunnigan Syndrome

histidine has been researched along with Dunnigan Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akinci, B; Altay, C; Cavdar, U; Demir, L; Demir, T; Kadioglu, P; Onay, H; Ozen, S; Savage, DB; Temeloglu, E; Uzum, AK	1

Other Studies

1 other study(ies) available for histidine and Dunnigan Syndrome

Article	Year
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations. Diabetic medicine : a journal of the British Diabetic Association, 2016, Volume: 33, Issue:10 Topics: Adult; Amino Acid Substitution; Codon; Family; Female; Histidine; Humans; Lamin Type A; Leucine; Lipodystrophy, Familial Partial; Male; Middle Aged; Mutation, Missense; Pedigree; Phenotype; PPAR gamma; Turkey	2016

Article

Year

Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations.

Diabetic medicine : a journal of the British Diabetic Association, 2016, Volume: 33, Issue:10

Topics: Adult; Amino Acid Substitution; Codon; Family; Female; Histidine; Humans; Lamin Type A; Leucine; Lipodystrophy, Familial Partial; Male; Middle Aged; Mutation, Missense; Pedigree; Phenotype; PPAR gamma; Turkey

2016